OXY TOTAL CARE CREAMY FACIAL CLEANSER- salicylic acid cream

Oxy by

Drug Labeling and Warnings

Oxy 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

Salicylic acid – Acne treatment

Keep Out of Reach of Children

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

Uses

• For the treatment of acne.
• Helps prevent new acne blemishes.

Warnings

For external use only.

When using this product

• keep away from 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, use only one topical acne medication at a time.

If pregnant or breast-feeding, ask a health professional before use.

Directions

• wet face
• dispense one to two pumps into your palm
• gently massage cleanser onto skin, avoiding eye area
• rinse thoroughly
• use one to two times daily
• Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.

Inactive Ingredients

water, sodium C14-16 olefin sulfonate, disodium cocoamphodiacetate, methyl gluceth-20, sodium cocoyl isethionate, disodium EDTA, fragrance, hydroxypropyltrimonium hyaluronate, PEG-7 glyceryl cocoate, PEG-8 dimethicone, potassium sorbate, sodium benzoate, triethanolamone

Questions?1-877-636-2677

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Package/Label Principal Display Panel

INGREDIENTS AND APPEARANCE

OXY  TOTAL CARE CREAMY FACIAL CLEANSER
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10742-1316
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 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
EDETATE DISODIUM (UNII: 7FLD91C86K)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10742-1316-1	148 mL in 1 TUBE; Type 0: Not a Combination Product	09/30/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/30/2019

Labeler - The Mentholatum Company (002105757)