Label: VIRCIN ADVANCED WART TREATMENT- salicylic acid cream
- NDC Code(s): 65121-397-15
- Packager: Pure Source, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
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Uses:
For the removal of plantar warts on the bottom of the foot. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness and the interruption of the footprint pattern. For the removal of common warts. The common wart is easily recognized by the rough “cauliflower-like” appearance of the surface.
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Warnings
on irritated skin, infected or reddened areas, moles, birthmarks, warts with hair growing from them, genital warts, warts on the face or mucous membrane. diabetes or poor blood circulation. Avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes. Stop use and ask a doctor if discomfort persists. Cap tube tightly and store at room temperature away from heat. For external use only.Do not useAsk a doctor before use if you haveAvoid inhaling vapors.Flammable. Keep away from fire and flame.
- Directions:
- Inactive Ingredients:
- VIRCIN Advanced wart treatment 0.5oz/14g (65121-397-15)
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INGREDIENTS AND APPEARANCE
VIRCIN ADVANCED WART TREATMENT
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65121-397 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 17 g in 100 g Inactive Ingredients Ingredient Name Strength BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ETHYL PYRUVATE (UNII: 03O98E01OB) GLYCERIN (UNII: PDC6A3C0OX) POVIDONE-IODINE (UNII: 85H0HZU99M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65121-397-15 1 in 1 CARTON 02/10/2017 1 14 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 06/12/2014 Labeler - Pure Source, LLC (080354456) Establishment Name Address ID/FEI Business Operations Pure Source, LLC 080354456 manufacture(65121-397)
