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.

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

Directions

Inactive ingredients

Water, Hydrated Silica, Glycerin, Dicaprylyl Carbonate, Cetearyl Alcohol, Magnesium Aluminum Silicate, Sodium Hydroxide, Cetearyl Glucoside, Butylene Glycol, Hydroxypropyl Starch Phosphate, Coco-Glucoside, Cedrus Atlantica Bark Extract, Portulaca Oleracea Extract, Xanthan Gum, Sodium Phytate, Sodium Benzoate, Benzyl Alcohol, Fragrance

Questions or comments?

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

Neutrogena®
naturals

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

Acne
Spot Treatment

Clinically proven acne medicine treats and helps
prevent breakouts

Fortified with an acne fighting bionutrient for clear,
healthy-looking skin

DERMATOLOGIST RECOMMENDED BRAND
SALICYLIC ACID ACNE TREATMENT

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)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Cetearyl Glucoside (UNII: 09FUA47KNA)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Coco Glucoside (UNII: ICS790225B)  
Cedrus Atlantica Bark (UNII: ITP1Q41UPF)  
Purslane (UNII: M6S840WXG5)  
Xanthan Gum (UNII: TTV12P4NEE)  
Phytate Sodium (UNII: 88496G1ERL)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Benzyl Alcohol (UNII: LKG8494WBH)  
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
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: 11/2012
Document Id: c6cc01eb-70a9-4c15-b627-c809ae66eb46
Set id: 49aa84ae-e1af-4ff7-8b86-a7411ea5bfee
Version: 1
Effective Time: 20121107
 
Neutrogena Corporation