Label: SALICYLIC ACID- wart remover gel gel
- NDC Code(s): 11822-0121-7
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Active ingredient
- Purpose
- Uses
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Warnings
For external use only.
Do not use
- on moles, birth marks and warts with hair growing from them
- on mucous membranes such as nose, anus, genitals and lips
- on irritated, infected or reddened skin
- on genital warts and warts on the face
- if you are diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist
When using this product
- if product gets into the eyes, flush with water for 15 minutes
- avoid inhaling vapors
- Directions
- Other information
- Inactive ingredients
- Questions?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SALICYLIC ACID
wart remover gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0121 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 7 g Inactive Ingredients Ingredient Name Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) ALCOHOL (UNII: 3K9958V90M) ETHYL ACETATE (UNII: 76845O8NMZ) HYPOPHOSPHOROUS ACID (UNII: 8B1RL9B4ZJ) HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P) POLYSORBATE 80 (UNII: 6OZP39ZG8H) PYROXYLIN (UNII: KYR8BR2X6O) CASTOR OIL (UNII: D5340Y2I9G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0121-7 7 g in 1 TUBE; Type 0: Not a Combination Product 10/07/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M028 10/07/2014 Labeler - Rite Aid Corporation (014578892)