PHISODERM ANTI-BLEMISH GEL CLEANSER- salicylic acid gel

Phisoderm Anti-Blemish Gel Cleanser by

Drug Labeling and Warnings

Phisoderm Anti-Blemish Gel Cleanser by is a Otc medication manufactured, distributed, or labeled by The Mentholatum Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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, lauramidopropyl betaine, sodium C14-16 olefin sulfonate, lauryl glucoside, trolamine, butylene glycol, chamomilla recutita (matricaria) flower extract, disodium EDTA, DMDM hydantoin, fragrance, glycerin, hydroxyphenyl propamidobenzoic acid, iodopropynyl butylcarbamate, lactic acid, pentylene glycol, polysorbate 20, sodium chloride

Questions?

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

Principal Display Panel

Principal Display Panel

INGREDIENTS AND APPEARANCE

PHISODERM ANTI-BLEMISH GEL CLEANSER 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10742-8417
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
TROLAMINE (UNII: 9O3K93S3TK)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CHAMOMILE (UNII: FGL3685T2X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10742-8417-1	177 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/01/2013

Labeler - The Mentholatum Company (002105757)