Label: SODIUM BICARBONATE 5 GR- sodium bicarbonate tablet
- NDC Code(s): 55681-307-02
- Packager: TWIN MED LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 12, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Do not use
- this product if you are on a sodium-restricted diet unless directed by a doctor
- Do not take more than 24 tablets for adults up to 60 years of age (or 12 tablets for adults 60 years of age or older) in a 24 hour period nor use maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.
- As with any drug, if you are pregnant or nursing a baby, seek advice of a health professional before using this product
Stomach Warning
- TO AVOID SERIOUS INJURY, D0 NOT TAKE UNTIL TABLET IS COMPLETELY DISSOLVED IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FULL FROM FOOD OR DRINK
- Consult a doctor if severe stomach pain occurs after taking this product.
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Directions
Adults:Take 1 tablet, dissolved in a glass of water, as needed. Maxlmum daily dose for adults up to 60 years of age is 24 tablets.
Maximum daily dose for adults 60 years of age or older is 12 tablets. Dissolve completely in water before drinking.
D0 NOT EXCEED RECOMMENDED DOSE
Not recommended for children.
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
SODIUM BICARBONATE 5 GR
sodium bicarbonate tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55681-307 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE 325 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) MINERAL OIL (UNII: T5L8T28FGP) Product Characteristics Color white Score 2 pieces Shape ROUND Size 8mm Flavor Imprint Code S32 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55681-307-02 200 in 1 BOTTLE; Type 0: Not a Combination Product 06/30/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 06/30/2022 Labeler - TWIN MED LLC (009579330)