NEUTROGENA SKINCLEARING MINERAL - BUFF- salicylic acid powder
NEUTROGENA SKINCLEARING MINERAL - CLASSIC IVORY- salicylic acid powder
NEUTROGENA SKINCLEARING MINERAL - NATURAL BEIGE- salicylic acid powder
NEUTROGENA SKINCLEARING MINERAL - NATURAL IVORY- salicylic acid powder
NEUTROGENA SKINCLEARING MINERAL - NUDE- salicylic acid powder
NEUTROGENA SKINCLEARING MINERAL - SOFT BEIGE- salicylic acid powder
NEUTROGENA SKINCLEARING MINERAL - TAN- salicylic acid powder
NEUTROGENA SKINCLEARING MINERAL - HONEY BEIGE- salicylic acid powder
Johnson & Johnson Consumer Inc.

----------

Neutrogena ® SkinClearing ® mineral powder (All 8 shades*)

Drug Facts

Active ingredients

Salicylic Acid (0.5%)

Purpose

Acne medication

Use

For the treatment of acne.

Warnings

For external use only.

When using this product

skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
if eye contact occurs, flush thoroughly with water.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

cleanse skin thoroughly before applying this product
cover the entire affected area with a thin layer one to three times daily
because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
if bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other information

Protect from Excessive Heat (40°C/104°F).

Inactive ingredients

Dimethicone, Zinc Stearate, Polyethylene, Octyldodecyl Stearoyl Stearate, C12-15 Alkyl Benzoate, Polysilicone-11, Nylon-12, Petrolatum, Ethylene/Acrylic Acid Copolymer, Calcium Silicate, Methylparaben, Sodium Dehydroacetate, Tocopheryl Acetate, Retinyl Palmitate, Propylparaben, Panthenol, Polymethyl Methacrylate, Ascorbyl Palmitate, C12-15 Alkyl Lactate, Cetyl Lactate, Benzalkonium Chloride, Cocamidopropyl PG-Dimonium Chloride Phosphate, Ascorbic Acid, Pantothenic Acid, Talc, Iron Oxides, Mica, Zinc Oxide.

May Contain: Titanium Dioxide, Carmine.

Questions?

Call toll-free 800-480-4812 or 215-273-8755 (collect) or visit www.neutrogena.com

Dist. by: JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Buff 30

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Buff 30

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Classic Ivory 10

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Classic Ivory 10

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Natural Beige 60

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Natural Beige 60

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Natural Ivory 20

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Natural Ivory 20

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Nude 40

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Nude 40

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Soft Beige 50

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Soft Beige 50

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Tan 80

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Tan 80

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Honey Beige 70

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

Principal Display Panel - 11 g Container Label - Honey Beige 70

NEUTROGENA SKINCLEARING MINERAL - BUFF
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0267
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
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)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0267-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009

NEUTROGENA SKINCLEARING MINERAL - CLASSIC IVORY
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0309
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
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)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0309-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009

NEUTROGENA SKINCLEARING MINERAL - NATURAL BEIGE
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0310
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
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)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0310-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009

NEUTROGENA SKINCLEARING MINERAL - NATURAL IVORY
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0268
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
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)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0268-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009

NEUTROGENA SKINCLEARING MINERAL - NUDE
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0266
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
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)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0266-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009

NEUTROGENA SKINCLEARING MINERAL - SOFT BEIGE
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0265
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
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)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0265-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009

NEUTROGENA SKINCLEARING MINERAL - TAN
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0311
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
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)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0311-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009	01/31/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009	01/31/2020

NEUTROGENA SKINCLEARING MINERAL - HONEY BEIGE
salicylic acid powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0264
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
PANTHENOL (UNII: WV9CM0O67Z)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
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)
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)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
PETROLATUM (UNII: 4T6H12BN9U)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
CALCIUM SILICATE (UNII: S4255P4G5M)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
METHYLPARABEN (UNII: A2I8C7HI9T)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69968-0264-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	11/30/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	11/30/2009

Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2024

Document Id: 0f3182d1-8bb1-9e5f-e063-6294a90ae0b2

Set id: 48bba584-b27f-4d92-b6ea-fb49fe8c3489

Version: 8

Effective Time: 20240117

Johnson & Johnson Consumer Inc.