Label: COMPOUND W MAXIMUM STRENGTH FAST ACTING LIQUID- salicylic acid liquid
- NDC Code(s): 63029-592-09
- Packager: Medtech Products Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 8, 2025
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
Flammable. Keep aware 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
- on irritated skin or on any area that is infected or reddened
- Directions
- Other Information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
COMPOUND W MAXIMUM STRENGTH FAST ACTING LIQUID
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63029-592 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.17 g in 9 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) CAMPHOR, (-)- (UNII: 213N3S8275) CASTOR OIL (UNII: D5340Y2I9G) LYTTA VESICATORIA (UNII: 3Q034RO3BT) ETHER (UNII: 0F5N573A2Y) ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B) HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ) MENTHOL, (+)- (UNII: C6B1OE8P3W) POLYSORBATE 80 (UNII: 6OZP39ZG8H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63029-592-09 1 in 1 CARTON 03/01/2014 1 9 g in 1 BOTTLE, WITH APPLICATOR; 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 03/01/2014 Labeler - Medtech Products Inc. (122715688)

