NDC Code(s) : 10812-514-11
Packager : Johnson & Johnson Consumer Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Neutrogena SkinClearing Mineral - TanSalicylic Acid POWDER
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10812-514
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Salicylic Acid(UNII: O414PZ4LPZ)
(Salicylic Acid - UNII:O414PZ4LPZ) 		Salicylic Acid5 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
Talc(UNII: 7SEV7J4R1U)
Dimethicone(UNII: 92RU3N3Y1O)
Zinc Stearate(UNII: H92E6QA4FV)
High Density Polyethylene(UNII: UG00KM4WR7)
Octyldodecyl Stearoyl Stearate(UNII: 3D47Q6D93C)
Mica(UNII: V8A1AW0880)
Alkyl (C12-15) Benzoate(UNII: A9EJ3J61HQ)
Nylon-12(UNII: 446U8J075B)
Petrolatum(UNII: 4T6H12BN9U)
Calcium Silicate(UNII: S4255P4G5M)
Sodium Dehydroacetate(UNII: 8W46YN971G)
Methylparaben(UNII: A2I8C7HI9T)
Vitamin A Palmitate(UNII: 1D1K0N0VVC)
.Alpha.-Tocopherol Acetate(UNII: 9E8X80D2L0)
Propylparaben(UNII: Z8IX2SC1OH)
Panthenol(UNII: WV9CM0O67Z)
Cocamidopropyl Propylene Glycol-Dimonium Chloride Phosphate(UNII: H2KVQ74JM4)
Cetyl Lactate(UNII: A7EVH2RK4O)
C12-15 Alkyl Lactate(UNII: GC844VRD7E)
Benzalkonium Chloride(UNII: F5UM2KM3W7)
Ascorbyl Palmitate(UNII: QN83US2B0N)
Pantothenic Acid(UNII: 19F5HK2737)
Ascorbic Acid(UNII: PQ6CK8PD0R)
Titanium Dioxide(UNII: 15FIX9V2JP)
Ferric Oxide Red(UNII: 1K09F3G675)
Zinc Oxide(UNII: SOI2LOH54Z)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:10812-514-1111 g in 1 CONTAINER Type 0: Not a Combination Product30/11/2009
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part333D 11/30/2009 12/01/2018

PRINCIPAL DISPLAY PANEL

Neutrogena
SkinClearing®
Mineral
Powder

MICROCLEAR®
- technology -

Principal Display Panel - 11 g Container Label