Label: THE ORDINARY SALICYLIC ACID 0.5%- salicylic acid lotion
- NDC Code(s): 72208-311-01
- Packager: Deciem Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
-
WARNINGS
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.
-
INDICATIONS & USAGE
Directions clean the skin thoroughly before applying
this product apply to body and rub in with hands if
needed allow the product to dry cover the entire affected
area with a thin layer one to three times daily because
excessive drying of the skin may occur, start with one
application daily, then gradually increase to two or three
times daily if needed or as directed by a doctor if
bothersome dryness or peeling occurs, reduce application
to once a day or every other day if eye contact occurs,
flush thoroughly with water. - QUESTIONS
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
THE ORDINARY SALICYLIC ACID 0.5%
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72208-311 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) CHLORPHENESIN (UNII: I670DAL4SZ) WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL DIMETHYLAMINE (UNII: L36BM7DG2T) GLYCERIN (UNII: PDC6A3C0OX) PROPANEDIOL (UNII: 5965N8W85T) SARCOSINE (UNII: Z711V88R5F) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72208-311-01 1 in 1 BOX 09/01/2024 1 240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 09/01/2024 Labeler - Deciem Inc (203133665) Establishment Name Address ID/FEI Business Operations Crystal Claire Cosmetics Inc. 205493484 analysis(72208-311) , manufacture(72208-311) , label(72208-311) , pack(72208-311)