Label: MAXIMUM STERNGTH CLEANSING PADS EQUATE- salicylic acid liquid
- NDC Code(s): 79903-207-01
- Packager: Walmart
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 11, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient Purpose
- PURPOSE
- Uses
- Warnings
- Do not use
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When using this product
keep away from eyes,lips, other mucous membranes. If contact occurs flush thoroughly with water • do not leave pad on skin for an extended period of time
Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
- Keep out of reach of children.
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Directions
cleanse the skin thoroughly before using the product • use the pad to clean and treat the entire affected area one to three times daily. Do not rinse. • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by doctor • if bothersome dryness or peeling occurs, reduce the application to once a day or every other day
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MAXIMUM STERNGTH CLEANSING PADS EQUATE
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-207 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) MENTHOL (UNII: L7T10EIP3A) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) SODIUM LAURYL SULFATE (UNII: 368GB5141J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-207-01 1 in 1 BOX 04/01/2024 1 90 in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 04/01/2024 Labeler - Walmart (051957769) Registrant - Bridgeview Investments LLC (035014854) Establishment Name Address ID/FEI Business Operations Derma Care Research Labs, LLC 116817470 manufacture(79903-207)