Neutrogena All-in-1 Acne Control Facial Treatment

Neutrogena All-in-1 Acne Control by

Drug Labeling and Warnings

Neutrogena All-in-1 Acne Control by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEUTROGENA ALL-IN-1 ACNE CONTROL  FACIAL TREATMENT- 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 All-in-1 Acne Control Facial Treatment

Drug Facts

Active ingredient

Salicylic Acid 1%

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

Inactive ingredients

Water
C12-15 Alkyl Benzoate
Cetearyl Alcohol
Glycerin
Dimethicone
PPG-10 Cetyl Ether
Arachidyl Alcohol
Methyl Gluceth-20
Glycine Soja (Soybean) Seed Extract
Behenyl Alcohol
Polyacrylamide
Isoceteth-20
Cetearyl Glucoside
Phenyl Trimethicone
Phenoxyethanol
Arachidyl Glucoside
C13-14 Isoparaffin
Benzyl Alcohol
Ethylene/Acrylic Acid Copolymer
Disodium EDTA
Fragrance
Ammonium Hydroxide
Methylparaben
Laureth-7
BHT
Ascorbyl Palmitate
Benzalkonium Chloride
Propylparaben
Polysorbate 20
Ethylparaben
Retinol
Lactobacillus/Soybean Seed Ferment Extract

Questions or comments?

1-800-582-4048 (USA only) or www.neutrogena.com

© Dist. by
Neutrogena Corporation
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

NEW
All-in-1
Acne
Control

facial treatment

clears up acne's
past, present & future

• Fades the look of past acne marks
• Clears present breakouts
• Helps prevent future breakouts

Neutrogena®

salicylic acid acne treatment

NET WT 1.0 OZ (28g)

NEUTROGENA ALL-IN-1 ACNE CONTROL   FACIAL TREATMENT
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10812-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ)	Salicylic Acid	10 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
Glycerin (UNII: PDC6A3C0OX)
Dimethicone (UNII: 92RU3N3Y1O)
PPG-10 CETYL ETHER (UNII: Q056X4917J)
Arachidyl Alcohol (UNII: 1QR1QRA9BU)
Methyl Gluceth-20 (UNII: J3QD0LD11P)
Soybean (UNII: L7HT8F1ZOD)
Docosanol (UNII: 9G1OE216XY)
Isoceteth-20 (UNII: O020065R7Z)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
Phenyl Trimethicone (UNII: DR0K5NOJ4R)
Phenoxyethanol (UNII: HIE492ZZ3T)
Arachidyl Glucoside (UNII: 6JVW35JOOJ)
C13-14 Isoparaffin (UNII: E4F12ROE70)
Benzyl Alcohol (UNII: LKG8494WBH)
ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
Edetate Disodium (UNII: 7FLD91C86K)
Ammonia (UNII: 5138Q19F1X)
Methylparaben (UNII: A2I8C7HI9T)
Laureth-7 (UNII: Z95S6G8201)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
Ascorbyl Palmitate (UNII: QN83US2B0N)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Propylparaben (UNII: Z8IX2SC1OH)
Polysorbate 20 (UNII: 7T1F30V5YH)
Ethylparaben (UNII: 14255EXE39)
Retinol (UNII: G2SH0XKK91)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10812-036-02	1 in 1 CARTON	08/01/2011	01/31/2020
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333D	08/01/2011	01/31/2020

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2019

Document Id: 88563636-32c1-44bf-b1f1-9bb901c98e00

34390-5

Set id: 6388e293-a2c7-4e58-adec-b10ca351b56b

Version: 3

Effective Time: 20191212

 

Johnson & Johnson Consumer Inc.