Label: MUCUS RELIEF IMMEDIATE RELEASE- guaifenesin 400mg tablet
- NDC Code(s): 50804-371-30
- Packager: Good Sense
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 5, 2021
If you are a consumer or patient please visit this version.
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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
you have
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
- cough accompanied by excessive phlegm (mucus)
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
- Directions
- Other information
- Storage
- Inactive ingredients
- Questions
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
MUCUS RELIEF IMMEDIATE RELEASE
guaifenesin 400mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-371 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 400 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) POVIDONE (UNII: FZ989GH94E) Product Characteristics Color white Score 2 pieces Shape OVAL Size 17mm Flavor Imprint Code AH370 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50804-371-30 1 in 1 CARTON 05/05/2021 1 30 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 12/23/2014 Labeler - Good Sense (076059836) Establishment Name Address ID/FEI Business Operations Allegiant Health 079501930 analysis(50804-371) , label(50804-371) , manufacture(50804-371) , pack(50804-371)