NDC Code 98132-754-01 | pharmacompass.com

NDC Code(s) : 98132-751-01, 98132-752-01, 98132-753-01, 98132-754-01, 98132-755-01, 98132-756-01, 98132-757-01, 98132-758-01, 98132-759-01, 98132-760-01
Packager : Orveon Global US, LLC

Category : HUMAN OTC DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-751
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-751-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-752
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-752-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-753
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-753-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-754
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-754-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-755
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-755-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-756
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-756-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-757
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-757-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-758
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-758-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-759
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:98132-759-01	1 in 1 BOX	01/01/2015
1		35 mL in 1 TUBE Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M020	01/01/2015

bareMinerals Complexion Rescue Broad Spectrum SPF 30 Titanium Dioxide LIQUID

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:98132-760
Route of Administration	TOPICAL	DEA Schedule

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE(UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	62 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER(UNII: 059QF0KO0R)
COCONUT ALKANES(UNII: 1E5KJY107T)
PROPANEDIOL(UNII: 5965N8W85T)
SQUALANE(UNII: GW89575KF9)
TREHALOSE(UNII: B8WCK70T7I)
ISOSTEARIC ACID(UNII: X33R8U0062)
GLYCERIN(UNII: PDC6A3C0OX)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
AGAR(UNII: 89T13OHQ2B)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
SALICORNIA EUROPAEA(UNII: 6ADL50JAKW)
COCO-CAPRYLATE/CAPRATE(UNII: 8D9H4QU99H)
BUTYLENE GLYCOL(UNII: 3XUS85K0RA)
LAUROYL LYSINE(UNII: 113171Q70B)
HYALURONATE SODIUM(UNII: YSE9PPT4TH)
POLYSORBATE 60(UNII: CAL22UVI4M)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
MAGNESIUM STEARATE(UNII: 70097M6I30)
MAGNESIUM HYDROXIDE(UNII: NBZ3QY004S)
MAGNESIUM CHLORIDE(UNII: 02F3473H9O)
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
POTASSIUM SORBATE(UNII: 1VPU26JZZ4)
PHENOXYETHANOL(UNII: HIE492ZZ3T)
FERRIC OXIDE RED(UNII: 1K09F3G675)