Label: STRIDEX SENSITIVE- salicylic acid liquid
- NDC Code(s): 10157-1007-1, 10157-1007-2, 10157-1007-3, 10157-1007-4
- Packager: Blistex Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- cleanse the skin thoroughly before applying medication
- use the pad to wipe the entire affected area
- repeat with a clean pad as necessary to remove remaining traces of dirt
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three times daily as 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
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL - 90 Pad Jar Carton
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INGREDIENTS AND APPEARANCE
STRIDEX SENSITIVE
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-1007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength aloe vera leaf (UNII: ZY81Z83H0X) ammonium lauryl sulfate (UNII: Q7AO2R1M0B) ammonium xylenesulfonate (UNII: 4FZY6L6XCM) citric acid monohydrate (UNII: 2968PHW8QP) DMDM hydantoin (UNII: BYR0546TOW) hamamelis virginiana top (UNII: UDA30A2JJY) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) PPG-5-ceteth-20 (UNII: 4AAN25P8P4) water (UNII: 059QF0KO0R) sodium borate (UNII: 91MBZ8H3QO) edetate sodium (UNII: MP1J8420LU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-1007-1 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:10157-1007-2 1 in 1 CARTON 12/01/2012 2 70 in 1 JAR 2 2 mL in 1 APPLICATOR; Type 0: Not a Combination Product 3 NDC:10157-1007-3 1 in 1 CARTON 12/01/2012 3 90 in 1 JAR 3 2 mL in 1 APPLICATOR; Type 0: Not a Combination Product 4 NDC:10157-1007-4 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(10157-1007)