PHISODERM CLEAR CONFIDENCE DAILY GEL FACE WASH- salicylic acid liquid
The Mentholatum Company

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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Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Uses

treats and helps prevent acne blemishes

Warnings

For external use only

When using this product

avoid contact with the eyes. If contact occurs, flush thoroughly with water.
skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet face, then gently massage onto skin
rinse well and pat dry
use twice daily

Inactive ingredients

water, sodium C14-16 olefin sulfonate, lauramidopropyl betaine, lauryl glucoside, sodium chloride, disodium EDTA, DMDM hydantoin, fragrance, iodopropynyl butylcarbamate, lactic acid, polysorbate 20, triethanolamine

Questions?

Toll free 1-877-636-2677 MON-FRI 9 AM-5 PM (EST)

Principal Display Panel

Phisoderm Clear Confidence Daily Gel Face Wash

Principal Display Panel

PHISODERM CLEAR CONFIDENCE DAILY GEL FACE WASH
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10742-1412
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DMDM HYDANTOIN (UNII: BYR0546TOW)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10742-1412-1	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	05/01/2012

Labeler - The Mentholatum Company (002105757)

Registrant - The Mentholatum Company (002105757)

Name	Address	ID/FEI	Business Operations
Establishment
The Mentholatum Company		002105757	manufacture(10742-1412)