Label: RAPIDOL SODIUM BICARBONATE- sodium bicarbonate powder
- NDC Code(s): 55758-319-04
- Packager: Pharmadel LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 18, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient & Purposes
- Uses For the relief of an upset stomach associated with these symptoms
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Warnings
Stomach Waring: To avoid serious injury, do not take powder until it 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.
Do not use
- the maximum daily dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor
- this product except under advice and supervision of a physician if you are allergic to milk or milk products
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Directions
- do not take more than your “ maximum daily dosage for your age group” in a 24-hour period. See Warnings.
- take a ½ teaspoon in a 4 fl. oz. (½ a glass) of water every 2 hours up to the maximum daily dosage or as directed by a doctor
- dissolve completely in water before drinking
age maximum daily dosage adults 60 years of age and over ½ teaspoon, 3 times a day adults under 60 and children 12 years of age and over ½ teaspoon, 6 times a day children under 12 years of age do not use - Other information
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
RAPIDOL SODIUM BICARBONATE
sodium bicarbonate powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55758-319 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE 2.6 g in 2.6 g Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55758-319-04 113 g in 1 BOTTLE; Type 0: Not a Combination Product 11/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 11/23/2020 Labeler - Pharmadel LLC (030129680)