Label: AIR POWER- guaifenesin tablet
- NDC Code(s): 53499-0232-1
- Packager: Schwabe North America, Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 30, 2023
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- Official Label (Printer Friendly)
- Active Ingredient:
- Inactive Ingredients:
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Dosage & Administration:
Adults & children 12 years and over: take 1-2 tablets every 4 hours, not to exceed 12 tablets in 24 hours
Children 6 to 11 years of age: take 1/2 to 1 tablet every 4 hours, not to exceed 6 tablets in 24 hours
Children under 6 years of age: consult a doctor before use
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Warnings:
Do not use this product if you are pregnant, attempting to become pregnant, or breast-feeding.
Do not take this product for persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema, or where cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.
- Ask a doctor:
- Stop Use:
- Keep out of Reach of Children:
- Overdosage:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AIR POWER
guaifenesin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53499-0232 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg Inactive Ingredients Ingredient Name Strength CARNAUBA WAX (UNII: R12CBM0EIZ) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) ICODEXTRIN (UNII: 2NX48Z0A9G) FENUGREEK SEED (UNII: 654825W09Z) GLYCERIN (UNII: PDC6A3C0OX) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) VERBASCUM THAPSUS LEAF (UNII: ANX0EG34JE) POVIDONE (UNII: FZ989GH94E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color brown (light brown to gray-brown w/ light and/or dark specks) Score no score Shape OVAL (Convex face, debossed 232 tablet) Size 20mm Flavor Imprint Code 232 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53499-0232-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 06/14/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 06/14/2021 Labeler - Schwabe North America, Inc (831153908) Establishment Name Address ID/FEI Business Operations Schwabe North America, Inc 831153908 manufacture(53499-0232)