Neutrogena® Naturals Acne Spot Treatment

Neutrogena Naturals Acne Spot Treatment by

Drug Labeling and Warnings

Neutrogena Naturals Acne Spot Treatment by is a Otc medication manufactured, distributed, or labeled by Neutrogena Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEUTROGENA NATURALS ACNE SPOT TREATMENT- salicylic acid lotion 
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® Naturals Acne Spot 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.
• 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

Store at Room Temperature.

Inactive ingredients

water, hydrated silica, glycerin, dicaprylyl carbonate, cetearyl alcohol, magnesium aluminum silicate, hydroxypropyl starch phosphate, coco-glucoside, benzyl alcohol, sodium benzoate, xanthan gum, cetearyl glucoside, sodium hydroxide, fragrance, sodium phytate, butylene glycol, cedrus atlantica bark extract, portulaca oleracea extract

Questions?

Call toll-free 800-582-4048 or 215-273-8755 (collect) or visit www.NeutrogenaNaturals.com

Dist. by Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 22 mL Tube Carton

NEW INFO

Neutrogena®
naturals

NO
harsh chemical
sulfates, parabens,
petrochemicals,
dyes, phthalates

Acne
Spot Treatment

Clinically proven acne medicine treats and helps
prevent breakouts

Fortified with Wintergreen leaf derived acne-fighting
Bionutrient for clear, healthy-looking skin

DERMATOLOGIST RECOMMENDED BRAND
SALICYLIC ACID ACNE TREATMENT
93% naturally derived

0.75 FL.OZ. (22mL)

NEUTROGENA NATURALS ACNE SPOT TREATMENT 
salicylic acid lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10812-024
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 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Hydrated Silica (UNII: Y6O7T4G8P9)
Glycerin (UNII: PDC6A3C0OX)
Dicaprylyl Carbonate (UNII: 609A3V1SUA)
Cetostearyl Alcohol (UNII: 2DMT128M1S)
Magnesium Aluminum Silicate (UNII: 6M3P64V0NC)
Coco Glucoside (UNII: ICS790225B)
Benzyl Alcohol (UNII: LKG8494WBH)
Sodium Benzoate (UNII: OJ245FE5EU)
Xanthan Gum (UNII: TTV12P4NEE)
Cetearyl Glucoside (UNII: 09FUA47KNA)
Sodium Hydroxide (UNII: 55X04QC32I)
Phytate Sodium (UNII: 88496G1ERL)
Butylene Glycol (UNII: 3XUS85K0RA)
Cedrus Atlantica Bark (UNII: ITP1Q41UPF)
Purslane (UNII: M6S840WXG5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10812-024-01	1 in 1 CARTON	11/01/2012	01/12/2019
1		22 mL 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	11/01/2012	01/12/2019

Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2019

Document Id: eb5c0439-964c-4f81-8b1d-101192cc7dfa

34390-5

Set id: 49aa84ae-e1af-4ff7-8b86-a7411ea5bfee

Version: 3

Effective Time: 20191205

 

Johnson & Johnson Consumer Inc.