Label: MUCUS RELIEF tablet, extended release
- NDC Code(s): 69168-459-02, 69168-459-75
- Packager: Allegiant Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 24, 2024
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- Official Label (Printer Friendly)
- Active ingredient(s)
- Purpose
- Use(s)
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Warnings
Ask a doctor before use if
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
- cough accompanied by too much phlegm (mucus)
- Directions
- Other information
- Inactive ingredients
- Questions/Comments
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
MUCUS RELIEF
mucus relief tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69168-459 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED) (UNII: K6MOM3T5YL) HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4) SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) Product Characteristics Color white Score no score Shape OVAL Size 16mm Flavor Imprint Code G;600 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69168-459-75 75 in 1 BOTTLE; Type 0: Not a Combination Product 04/24/2024 2 NDC:69168-459-02 150 in 1 BOTTLE; Type 0: Not a Combination Product 04/24/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA213420 04/24/2024 Labeler - Allegiant Health (079501930)