Label: BIORE WITCH HAZEL PORE CLARIFYING TONER- salicylic acid liquid
- NDC Code(s): 10596-187-80
- Packager: Kao USA Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 1, 2025
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
- Cleanse skin thoroughly before applying medication.
- Cover the entire affected area with a thin layer 1 to 3 times daily using a cotton ball or pad.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to 2 or 3 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.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
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SPL UNCLASSIFIED SECTION
what it does:
BIORE PORE CLARIFYING TONER teams up with Witch Hazel & Salicylic Acid. This refreshing formula helps restore skin's balance as it penetrates and deep cleans pores for clear skin.
Questions? 1-888-BIORE-11
www.biore.com
BIORE is a trademark of Kao Corp.
Distributed by Kao USA Inc.
Cincinnati, OH 45214 ©2018
Made in Canada
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BIORE WITCH HAZEL PORE CLARIFYING TONER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10596-187 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 ALCOHOL (UNII: 3K9958V90M) ISOPROPYL ALCOHOL (UNII: ND2M416302) WITCH HAZEL (UNII: 101I4J0U34) BENZOPHENONE (UNII: 701M4TTV9O) EDETATE DISODIUM (UNII: 7FLD91C86K) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) POLYSORBATE 20 (UNII: 7T1F30V5YH) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CITRATE (UNII: 1Q73Q2JULR) MENTHOL (UNII: L7T10EIP3A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10596-187-80 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/18/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/18/2018 Labeler - Kao USA Inc. (004251617)