NEUTROGENA NATURALS ACNE SPOT TREATMENT- salicylic acid lotion 
Neutrogena Corporation

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

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)

Principal Display Panel - 22 mL Tube Carton
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 DEA Schedule     
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
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
Labeler - Neutrogena Corporation (008254617)

Revised: 6/2015
Document Id: a49de6ff-a4e0-4eea-ba16-4d9befe431ff
Set id: 49aa84ae-e1af-4ff7-8b86-a7411ea5bfee
Version: 2
Effective Time: 20150624
 
Neutrogena Corporation