Label: STRIDEX ESSENTIAL- salicylic acid liquid
- NDC Code(s): 10157-2119-1
- Packager: Blistex Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 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 - 55 Pad Jar Carton
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INGREDIENTS AND APPEARANCE
STRIDEX ESSENTIAL
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-2119 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 1 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Ammonium Xylenesulfonate (UNII: 4FZY6L6XCM) Ammonium Lauryl Sulfate (UNII: Q7AO2R1M0B) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) Phenoxyethanol (UNII: HIE492ZZ3T) Ethylhexylglycerin (UNII: 147D247K3P) Sodium Hydroxide (UNII: 55X04QC32I) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Sodium Ascorbyl Phosphate (UNII: 836SJG51DR) EDETATE SODIUM (UNII: MP1J8420LU) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-2119-1 1 in 1 CARTON 12/06/2022 1 55 in 1 JAR 1 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 12/06/2022 Labeler - Blistex Inc (005126354) Establishment Name Address ID/FEI Business Operations Blistex Inc 005126354 MANUFACTURE(10157-2119)