Label: STRIDEX MAXIMUM- salicylic acid liquid
- NDC Code(s): 10157-1006-1, 10157-1006-2, 10157-1006-3, 10157-1006-4
- Packager: Blistex Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- clean the skin thoroughly before applying this product
- use the pad to cover the entire affected area with a 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 or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- do not leave pad on skin for an extended period of time
- keep away from eyes, lips and other mucous membranes
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL - 90 Pad Jar Carton
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INGREDIENTS AND APPEARANCE
STRIDEX MAXIMUM
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-1006 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 in 100 mL Inactive Ingredients Ingredient Name Strength AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) DIMETHICONOL/TRIMETHYLSILOXYSILICATE CROSSPOLYMER (40/60 W/W; 1000000 PA.S) (UNII: 83D19O7250) SODIUM BORATE (UNII: 91MBZ8H3QO) EDETATE SODIUM (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-1006-1 1 in 1 CARTON 12/01/2012 1 55 in 1 JAR 1 2 mL in 1 APPLICATOR; Type 0: Not a Combination Product 2 NDC:10157-1006-2 1 in 1 CARTON 12/01/2012 2 90 in 1 JAR 2 2 mL in 1 APPLICATOR; Type 0: Not a Combination Product 3 NDC:10157-1006-3 1 in 1 CARTON 12/01/2012 3 70 in 1 JAR 3 2 mL in 1 APPLICATOR; Type 0: Not a Combination Product 4 NDC:10157-1006-4 1 in 1 CARTON 12/01/2012 4 110 in 1 JAR 4 2 mL in 1 APPLICATOR; 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 12/01/2012 Labeler - Blistex Inc. (005126354) Establishment Name Address ID/FEI Business Operations Blistex Inc. 005126354 MANUFACTURE(10157-1006)