Label: GLYCYLIC- salicylic acid liquid
- NDC Code(s): 49406-009-15
- Packager: The Tetra Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 12, 2023
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
FOR EXTERNAL USE ONLY.
Flammable
• keep away from fire or flame.
• cap bottle tightlyand store at room temperature away from heat.Do not use
• if you are a diabetic or have poor blood circulation, except under the advice and supervision of a doctor or podiatrist.
• irritated, infected or reddened skin.
• genital warts and warts on the face.
• moles, birthmarks and warts with hair growing from them.
• mucous membranes.When using this product
• avoid contact with eyes. If product gets into the eyes, flush with water for 15 minutes.
• avoid inhaling vapors.Stop use and ask doctor if
• discomfort persists. - Keep out of reach of children
- Directions
- Inactive ingredients
- Product label
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INGREDIENTS AND APPEARANCE
GLYCYLIC
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49406-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 17 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) IODINE (UNII: 9679TC07X4) GLYCOLIC ACID (UNII: 0WT12SX38S) ETHYL PYRUVATE (UNII: 03O98E01OB) ALCOHOL (UNII: 3K9958V90M) PYROXYLIN (UNII: KYR8BR2X6O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49406-009-15 1 in 1 BOX 07/01/2022 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 07/01/2022 Labeler - The Tetra Corporation (829958409)