NEUTROGENA SKINCLEARING MINERAL POWDER - HONEY 85- salicylic acid cream
NEUTROGENA SKINCLEARING MINERAL POWDER - CHESTNUT 135- salicylic acid cream
Johnson & Johnson Consumer Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Neutrogena SkinClearing Mineral pressed Powder

Drug Facts

Active ingredient

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.

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

Directions

Clean the 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

Distributed by: JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558 © J&JCI 2017

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Honey 85

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Honey 85

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Chestnut 135

Neutrogena
SkinClearing ®
mineral
powder

MICRO CLEAR ®
- technology -

PRINCIPAL DISPLAY PANEL - 11 g Container Label - Chestnut 135

NEUTROGENA SKINCLEARING MINERAL POWDER - HONEY 85
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0339
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:69968-0339-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	10/02/2017	01/31/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	10/02/2017	01/31/2021

NEUTROGENA SKINCLEARING MINERAL POWDER - CHESTNUT 135
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69968-0340
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:69968-0340-1	11 g in 1 CONTAINER; Type 0: Not a Combination Product	10/02/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	10/02/2017

Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023

Document Id: ee825456-25e4-77e9-e053-2a95a90a8b77

Set id: ab044422-db53-43de-b106-cfe1a523e4e9

Version: 6

Effective Time: 20230113

Johnson & Johnson Consumer Inc.