Label: GUAIFENESIN tablet
- NDC Code(s): 68196-405-14
- Packager: SAM'S WEST INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 18, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (in each extended-release bi-layer tablet)
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children.
- Directions
- Other Information
- Inactive ingredients
- Questions?
- PDP
-
INGREDIENTS AND APPEARANCE
GUAIFENESIN
guaifenesin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68196-405 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 MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208) SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D) HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4) Product Characteristics Color white Score no score Shape OVAL ((Elliptical)) Size 22mm Flavor Imprint Code G;1200 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68196-405-14 56 in 1 BLISTER PACK; Type 0: Not a Combination Product 10/06/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA213420 10/06/2023 Labeler - SAM'S WEST INC (051957769)