Label: MUCA CLEAR- guaifenesin tablet
- NDC Code(s): 59800-1365-1
- Packager: Schwabe North America, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 21, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Inactive Ingredient
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Dosage & Administration
adults & children 12 years of age and older: take 1-2 tablets every 4 hours, not to exceed 12 tablets in 24 hours
children 6 - 11 years of age: take 1/2 - 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 be pregant, 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 Doctor
- Stop Use
- Keep out of reach of children
- Overdosage
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MUCA CLEAR
guaifenesin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59800-1365 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) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MULLEIN LEAF (UNII: 9936O846LI) POVIDONE (UNII: FZ989GH94E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color brown (pale yellow to brown with 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:59800-1365-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 09/24/2020 Labeler - Schwabe North America, Inc (831153908) Establishment Name Address ID/FEI Business Operations Schwabe North America, Inc 831153908 manufacture(59800-1365)