Label: MUCUS RELIEF- guaifenesin 400 mg tablet
- NDC Code(s): 72090-035-01
- Packager: Pioneer Life Sciences, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 29, 2024
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- Active ingredient (in each tablet)
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
MUCUS RELIEF
guaifenesin 400 mg tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72090-035 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 SILICON DIOXIDE (UNII: ETJ7Z6XBU4) POVIDONE (UNII: FZ989GH94E) MALTODEXTRIN (UNII: 7CVR7L4A2D) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape capsule Size 14mm Flavor Imprint Code C16 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72090-035-01 200 in 1 BOTTLE; Type 0: Not a Combination Product 08/29/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 08/29/2024 Labeler - Pioneer Life Sciences, LLC (014092742)