Label: ATRIX CLARIFYING TONER- salicylic acid liquid
- NDC Code(s): 59088-444-08
- Packager: PureTek Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 2, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
Flammable: Keep away from fire or flame.
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Directions
■ Clean the skin thoroughly before applying product ■ moisten a cotton ball and 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.
Use under the direction of a medical practitioner.
- Other information
- QUESTIONS
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Inactive ingredients
Aqua (Purified Water), Benzalkonium Chloride, Benzyl Alcohol, Citrus Paradisi (Grapefruit) Peel Oil, Ethoxydiglycol, Ethyl Alcohol, Glycerin, Menthol, Menthyl Lactate, Pyrus Malus (Apple) Fruit Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Sambucus Nigra (Elderberry) Fruit Extract, Sodium Hydroxide.
- Atrix™ Clarifying Toner
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INGREDIENTS AND APPEARANCE
ATRIX CLARIFYING TONER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-444 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BENZYL ALCOHOL (UNII: LKG8494WBH) GRAPEFRUIT OIL (UNII: YR377U58W9) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) APPLE (UNII: B423VGH5S9) ROSEMARY (UNII: IJ67X351P9) EUROPEAN ELDERBERRY (UNII: BQY1UBX046) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59088-444-08 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/05/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 01/05/2021 Labeler - PureTek Corporation (785961046)