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
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated May 11, 2023
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- 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 final part358B 03/01/2014 Labeler - Medtech Products Inc. (122715688)