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QUICK DRY ACNE TREATMENT

Medically reviewed on December 4, 2017

Dosage form: lotion
Ingredients: SULFUR 10g in 100mL
Labeler: DR. THROWER'S SKINCARE, INC.
NDC Code: 69299-101

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.

ACTIVE INGREDIENTS:

SULFUR- 10.0%

ZINC OXIDE- 5.0%

PURPOSE:

TREATS ACNE AND SHAVE BUMPS

USES:
  • DRIES UP EXCESS OIL
  • CLEARS UP ACNE AND SHAVING BUMPS

DIRECTIONS:

USE EVENINGS. SHAKE TO ACTIVATE

APPLY TO CLEAN SKIN AFTER SPF 30 IN AM OR ALOE MOISTURIZING CREAM IN PM

APPLY DIRECTLY TO THE ACNE OR SHAVING BUMPS WITH A COTTON SWAB.

ALLOW TO DRY FOR APPROXIMATELY 5-10 MINTUES AND LEAVE ON OVERNIGHT.

INACTIVE INGREDIENTS:

ETHYL ALCOHOL, AQUA, SPIRAEA ULMARIA EXTRACT, CINNAMOMUM CAMPHORA OIL, MAGNESIUM ALUMINIUM SILICATE, PIGMENT YELLOW 42, PIGMENT BLACK11, PIGMENT RED 101, PEG-8 DIMETHICONE, GLYCERINE, OCTYLDODECANOL, RETINYL PALMITATE (VITAMIN A), TOCOPHERYL ACETATE (VITAMIN E),  ASCORBIC ACID (VITAMIN C), PYRIDOXINE HCL (VITAMIN B6), SILICA, SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA, CHOLECALCIFEROL

KEEP  OUT OF REACH OF CHILDREN.

WARNINGS

FOR EXTERNAL USE ONLY

QUICK DRY ACNE TREATMENT 
sulfur lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69299-101
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SULFUR (SULFUR) SULFUR10 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ZINC OXIDE 
ALCOHOL 
WATER 
FILIPENDULA ULMARIA WHOLE 
CAMPHOR OIL 
MAGNESIUM ALUMINUM SILICATE 
FERRIC OXIDE YELLOW 
FERROSOFERRIC OXIDE 
FERRIC OXIDE RED 
PEG-8 DIMETHICONE 
GLYCERIN 
OCTYLDODECANOL 
VITAMIN A PALMITATE 
.ALPHA.-TOCOPHEROL ACETATE 
ASCORBIC ACID 
PYRIDOXINE HYDROCHLORIDE 
SILICON DIOXIDE 
SODIUM PROPOXYHYDROXYPROPYL THIOSULFATE SILICA 
CHOLECALCIFEROL 
Packaging
#Item CodePackage Description
1NDC:69299-101-511 BOTTLE in 1 BOX
1NDC:69299-101-1130 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D11/17/2014
Labeler - DR. THROWER'S SKINCARE, INC. (078711495)
Registrant - DR. THROWER'S SKINCARE, INC. (078711495)

 
DR. THROWER'S SKINCARE, INC.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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