NDC Code(s) : 10812-510-11
Packager : Johnson & Johnson Consumer Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Neutrogena SkinClearing Mineral - BuffSalicylic Acid POWDER
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10812-510
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)
BENZALKONIUM CHLORIDE(UNII: F5UM2KM3W7)
ASCORBYL PALMITATE(UNII: QN83US2B0N)
PANTOTHENIC ACID(UNII: 19F5HK2737)
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:10812-510-1111 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