PERSONAL CARE DEEP CLEANING ASTRINGENT- salicylic acid liquid 
Delta Brands & Products LLC

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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Drug Facts

Active Ingredient

Salicylic Acid 0.5%

Purpose

Acne treatment

Use

for the treatment of acne

Warnings

For external use only Keep out of eyes ■ If contact with eyes occurs, immediately flush with water.

Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug should be used unless directed by a doctor.

Keep out of reach of children

If accidentally ingested seek medical help immediately or contact your local Poison Control Center.

Directions

■ use twice a day ■ wet face ■ apply to hands, add water and work into a lather ■ massage face gently,then rinse thoroughly.

Inactive Ingredients

water (aqua), alcohol (24.5%), propylene glycol, glycerin, PEG-32, algae extract, DMDM hydantoin, dimethicone propyl PG-betaine, sodium citrate, aloe barbadensis leaf extract, benzophenone-4, fragrance, FD&C yellow No. 5.

Package Label

Package Label

PERSONAL CARE  DEEP CLEANING ASTRINGENT
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72133-200
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SULISOBENZONE (UNII: 1W6L629B4K)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72133-200-08237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/09/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D04/09/2018
Labeler - Delta Brands & Products LLC (080999173)

Revised: 4/2018
Document Id: 69aea957-68c8-244c-e053-2a91aa0a8f5b
Set id: 69aea957-68c7-244c-e053-2a91aa0a8f5b
Version: 1
Effective Time: 20180412
 
Delta Brands & Products LLC