Label: CLEARSKIN BLEMISH CLEARING SPOT TREATMENT- salicylic acid gel
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0223-1, 10096-0223-2 - Packager: Avon Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated June 14, 2010
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use onlyWhen using this product
- avoid contact with eyes. If product contacts eyes, rinse thoroughly with water.
- using other topical acne medications at the same time or immediately after this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
- avoid contact with eyes. If product contacts eyes, rinse thoroughly with water.
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DOSAGE & ADMINISTRATION
Directions
- cleanse skin thoroughly before applying medication
- cover the entire affected area with thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily if needed or as directed by a doctor
- if bothersome dryness, irritation or peeling occurs, reduce application to once a day or every other day
- cleanse skin thoroughly before applying medication
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INACTIVE INGREDIENT
Inactive ingredients
WATER/EAU
SD ALCOHOL 40-B
PROPYLENE GLYCOL
ETHOXYDIGLYCOL
TRIDECETH-9
HYDROXYETHYLCELLULOSE
TRITICUM VULGARE (WHEAT) GERM EXTRACT
PUNICA GRANATUM FRUIT JUICE
ALOE BARBADENSIS LEAF JUICE
CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT
HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT
XANTHAN GUM
DISODIUM EDTA
AMMONIUM HYDROXIDE
PARFUM/FRAGRANCE - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEARSKIN BLEMISH CLEARING SPOT TREATMENT
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0223 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic acid (UNII: O414PZ4LPZ) (Salicylic acid - UNII:O414PZ4LPZ) Salicylic acid 0.3 mL in 15 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0223-2 1 in 1 CARTON 1 NDC:10096-0223-1 15 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 06/14/2010 Labeler - Avon Products, Inc. (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 005149471 manufacture