NEUTROGENA STUBBORN ACNE SPOT DRYING- sulfur 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 Stubborn Body Acne Cleanser and Exfoliator

Drug Facts

Active ingredient

Sulfur 10%

Purpose

Acne treatment

Use

For the treatment of acne.

Warnings

For external use only.

Flammable: Keep away from fire or flame

When using this product

  • Avoid contact with eyes. If contact occurs, immediately flush with water.
  • 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.
  • apply only to areas with acne.

Do not use on

▪ broken skin ▪ large areas of the skin

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

Directions

­­­­­­­­­­­­­­­­­­­­­­­­­­­­­­

Other Information

Inactive ingredients

Isopropyl Alcohol, Water, Calamine, Niacinamide, Zinc Oxide, Zea Mays (Corn) Starch, Magnesium Aluminum Silicate, Salicylic Acid, Titanium Dioxide

Questions?

800-582-4048; outside US, dial collect 215-273-8755 or visit www.neutrogena.com

Distributed by:

JOHNSON & JOHNSON

CONSUMER INC.


Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 29mL Bottle

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

NEW

STUBBORN

ACNE

SPOT DRYING LOTION

Sulfur Acne Treatment

10% Sulfur +

4% Niacinamide

Fragrance Free

clears acne by drying up

and shrinking pimples

1 FL OZ (29mL)

Neutrogena-001

NEUTROGENA STUBBORN ACNE SPOT DRYING 
sulfur lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0761
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ZINC OXIDE (UNII: SOI2LOH54Z)  
STARCH, CORN (UNII: O8232NY3SJ)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
NIACINAMIDE (UNII: 25X51I8RD4)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0761-11 in 1 CARTON08/01/2022
129 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D08/01/2022
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ef3c381a-33ef-ee17-e053-2a95a90abd43
Set id: dffe9bf4-a8a2-4fa0-e053-2995a90abcb3
Version: 2
Effective Time: 20230113
 
Johnson & Johnson Consumer Inc.