Label: COMPOUND W- salicylic acid gel gel
- NDC Code(s): 51142-595-12
- Packager: ASO LLC
- This is a repackaged label.
- Source NDC Code(s): 49354-076
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE
-
WARNINGS
For external use only.
Flammable. Keep away from fire and flame.
Do not use
- on irritated skin or on any area that is infected or reddened.
- on moles, birthmarks, warts with hair growing from them, genital warts or warts on the face or mucous membranes.
- if you have diabetes or poor blood circulation.
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
COMPOUND W
salicylic acid gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51142-595(NDC:49354-076) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 170 mg in 1 g Inactive Ingredients Ingredient Name Strength ETHYL ACETATE (UNII: 76845O8NMZ) CAMPHOR (NATURAL) (UNII: N20HL7Q941) CASTOR OIL (UNII: D5340Y2I9G) HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ALCOHOL (UNII: 3K9958V90M) HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P) ISOPROPYL ALCOHOL (UNII: ND2M416302) PYROXYLIN (UNII: KYR8BR2X6O) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51142-595-12 1 in 1 CARTON 12/01/2020 1 7 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 12/01/2020 Labeler - ASO LLC (152793493)