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OXY CLINICAL(salicylic acid) liquid
2014-03-02 19:16:16 来源: 作者: 【 】 浏览:409次 评论:0

Active ingredient

Salicylic acid 2%

Purpose

Salicylic acid - 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.
  • using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug should be used unless directed by a doctor.

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
  • use twice daily

Inactive ingredients

acrylates copolymer, anhydrous citric acid, astragalus membranaceus root extract, C8-22 alkyl acrylates/methacrylic acid crosspolymer, caprylyl glycol, cocamidopropyl betaine, edetate disodium, forsythia suspensa fruit extract, fragrance, glycerin, methyl gluceth-20, PEG/PPG-8/3 diisostearate, phenoxyethanol, polysorbate 20, potassium sorbate, purified water, sodium benzoate, sodium C14-16 olefin sulfonate, sorbic acid, trolamine

Questions?

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

Package/Label Principal Display Panel

OXY Clinical Advanced Face Wash Acne Treatment Clinical results without a prescription

OXY Clinical Advanced Face Wash

Acne Treatment

2% Salicylic Acid

Clinical results without a prescription

The Mentholatum Company

Orchard Park, NY 14127


OXY CLINICALADVANCED FACE WASH
salicylic acid liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 10742-8214
Route of Administration TOPICAL DEA Schedule  
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALICYLIC ACID(SALICYLIC ACID) SALICYLIC ACID 20mg in1mL
Inactive Ingredients
Ingredient Name Strength
No Inactive Ingredients Found
Product Characteristics
Color   Score  
Shape   Size  
Flavor   Imprint Code  
Contains  
Packaging
# NDC Package Description Multilevel Packaging
1 10742-8214-1 150mLIn1BOTTLE None
2 10742-8214-2 118mLIn1BOTTLE None
3 10742-8214-3 59mLIn1BOTTLE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333 06/01/2010  

Labeler -The Mentholatum Company(002105757) 
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