- claims
- active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children
-
Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- because excessice 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 daily application to once a day or evey other day
- Inactive ingredients
- Adverse reactions
- Principal display panel
-
INGREDIENTS AND APPEARANCE
OIL-FREE ASTRINGENT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0104 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 18 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) ISOCETETH-20 (UNII: O020065R7Z) POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A) SULISOBENZONE (UNII: 1W6L629B4K) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0869-0104-34 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/03/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 08/03/2016 Labeler - Vi-Jon, LLC (790752542) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0869-0104)