Label: AIR POWER- guaifenesin tablet
- NDC Code(s): 53499-0232-1
- Packager: Schwabe North America, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 1, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient:
- Inactive Ingredients:
-
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 ½ 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
- Warnings:
- Ask a doctor:
- Stop Use:
- Keep out of Reach of Children:
- Overdosage:
- PRINCIPAL DISPLAY PANEL
-
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) FENUGREEK SEED (UNII: 654825W09Z) GLYCERIN (UNII: PDC6A3C0OX) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) 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)