BIORE WITCH HAZEL PORE CLARIFYING CLEANSER- salicylic acid liquid 
Kao USA Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Biore Witch Hazel Pore Clarifying Cooling Cleanser

BIORE PORE CLARIFYING COOLING CLEANSER

This refreshingly cool formula works to deep clean by removing over 99% of blemish causing dirt and oil.

Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Uses

Warnings

For external use only.

When using this product

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

store at room temperature

Inactive ingredients

water, glycerin, sodium C14-16 olefin sulfonate, sodium laureth sulfate, coco-glucoside, cocamidopropyl betaine, betaine, lauric acid, PEG-7 glyceryl cocoate, glyceryl oleate, sodium hydroxide, fragrance, menthol, polyquaternium-7, BHT, disodium EDTA, hamamelis virginiana (witch hazel) water, eucalyptus globulus leaf extract, lavandula angustifolia (lavender) flower extract, alcohol

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

Biore

free your pores!

WITCH HAZEL

deep cleans, clarifies and refines pores

PORE CLARIFYING COOLING CLEANSER

SALICYLIC ACID ACNE TREATMENT

oil-free

acne's outta here!

6.77 FL OZ (200 mL)

10596-188 03-2021

BIORE  WITCH HAZEL PORE CLARIFYING CLEANSER
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10596-188
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERYL OLEATE (UNII: 4PC054V79P)  
WITCH HAZEL (UNII: 101I4J0U34)  
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
COCO GLUCOSIDE (UNII: ICS790225B)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
MENTHOL (UNII: L7T10EIP3A)  
BETAINE (UNII: 3SCV180C9W)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
LAURIC ACID (UNII: 1160N9NU9U)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10596-188-67200 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product12/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D12/01/2018
Labeler - Kao USA Inc. (004251617)

Revised: 3/2021
Document Id: bda8ad18-76ac-1ccb-e053-2a95a90a06e6
Set id: 7c107414-457b-1ab0-e053-2991aa0af55a
Version: 3
Effective Time: 20210316
 
Kao USA Inc.