Label: PANOXYL CLARIFYING EXFOLIANT- salicylic acid liquid
- NDC Code(s): 0316-0296-04
- Packager: Crown Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 26, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
- shake well before using
- clean the skin thoroughly before applying this product
- using a cotton pad, cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Other information
- Inactive ingredients
- Questions or comments?
- Panoxyl Clarifying Exfoliant Bottle
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INGREDIENTS AND APPEARANCE
PANOXYL CLARIFYING EXFOLIANT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0316-0296 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength BETAINE (UNII: 3SCV180C9W) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) PENTYLENE GLYCOL (UNII: 50C1307PZG) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PROPANEDIOL (UNII: 5965N8W85T) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBIC ACID (UNII: X045WJ989B) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0316-0296-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/02/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/01/2023 Labeler - Crown Laboratories, Inc. (079035945) Establishment Name Address ID/FEI Business Operations Crown Laboratories, Inc. 079035945 manufacture(0316-0296)