Label: UP AND UP MUCUS RELIEF- guaifenesin tablet, extended release
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Contains inactivated NDC Code(s)
NDC Code(s): 11673-325-30, 11673-325-66 - Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 7, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each extended-release tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
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- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
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- cough accompanied by too much phlegm (mucus)
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Directions
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- do not crush, chew, or break tablet
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- take with a full glass of water
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- this product can be administered without regard for the timing of meals
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- adults and children 12 years of age and over: 1 tablet every 12 hours. Do not exceed 2 tablets in 24 hours.
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- children under 12 years of age: do not use
- Other information
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
UP AND UP MUCUS RELIEF
guaifenesin tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-325 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 1200 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) COPOVIDONE K25-31 (UNII: D9C330MD8B) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color BLUE (Light Blue) Score no score Shape OVAL (Biconvex) Size 22mm Flavor Imprint Code Watson;1200 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-325-66 1 in 1 CARTON 07/11/2016 11/30/2019 1 14 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:11673-325-30 1 in 1 CARTON 07/11/2016 07/02/2018 2 28 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA091009 07/11/2016 Labeler - Target Corporation (006961700)