OXY SKIN CLEARING SOOTHING CLEANSER DAILY DEFENSE- 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 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 cleanser onto skin
•: rinse well and pat dry
•: Sensitivity Test: Apply product sparingly to a small affected area for the first 3 days. If no discomfort occurs, follow directions above.

Inactive ingredients

aloe barbadensis leaf juice, ascorbic acid, astragalus membranaceus root extract, butylene glycol, butyl methoxydibenzoylmethane, caprylyl glycol, cucumis sativus (cucumber) fruit extract, DMDM hydantoin, edetate disodium, ethylhexyl methoxycinnamate, ethylhexyl salicylate, forsythia suspensa fruit extract, fragrance, green 3, iodopropynyl butylcarbamate, lactic acid, lauramidopropyl betaine, lauryl glucoside, menthol, octyldodecanol, PEG-8 dimethicone, PEG-150 distearate, PEG-40 hydrogenated castor oil, phenoxyethanol, polysorbate 20, PPG-26-buteth-26, purified water, retinyl palmitate, silica, sodium C14-16 olefin sulfonate, sodium chloride, sodium propoxyhydroxypropyl thiosulfate silica, sorbic acid, tocopheryl acetate, trolamine, yellow 5

Questions?

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

Package/Label Principal Display Panel

Principal Display Panel

Drug Facts

OXY SKIN CLEARING SOOTHING CLEANSER DAILY DEFENSE
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:10742-1361
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
AVOBENZONE (UNII: G63QQF2NOX)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CUCUMBER (UNII: YY7C30VXJT)
DMDM HYDANTOIN (UNII: BYR0546TOW)
EDETATE DISODIUM (UNII: 7FLD91C86K)
OCTINOXATE (UNII: 4Y5P7MUD51)
OCTISALATE (UNII: 4X49Y0596W)
FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
OCTYLDODECANOL (UNII: 461N1O614Y)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
WATER (UNII: 059QF0KO0R)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SORBIC ACID (UNII: X045WJ989B)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:10742-1361-1	207 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2015	10/31/2017
2	NDC:10742-1361-2	248 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2015	10/31/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	02/01/2015	10/31/2017

Labeler - The Mentholatum Company (002105757)

Revised: 8/2017

Document Id: ff2def1d-2dbb-44a3-8ab5-976fcec01d9f

Set id: 0a7ab6a0-7d82-4168-a896-f9f8740869f5

Version: 2

Effective Time: 20170824

The Mentholatum Company