D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO- sodium bicarbonate powder

D-D SUDIUM BICARBONATE U.S.P. by

Drug Labeling and Warnings

D-D SUDIUM BICARBONATE U.S.P. by is a Otc medication manufactured, distributed, or labeled by Evi Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Sodium Bicarbonate U.S.P. 100%

Purpose

Antacid

Uses

For the relief of heartburn, sour stomach, acid indigestion, and upset stomach associated with these symptoms.

Warnings

Do not exceed the maximum daily dosage. Do not take more than four 1/4 teaspoonfuls in 24 hours. Do not use the maximum dosage of this product for more than 2 weeks.

Do not use if you are on a sodium-restricted diet.

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children

In case of overdose, get medical help or contact aPoison Control Center right away

Directions

Adults and children 12 years of age and over: Mix 1/4 teaspoonful in water and drink.

Do not use more than 4 times a day. For children under 12 years of age, ask a doctor.

Other Information

Store at controlled room temperature 15º-25ºC (59º-86ºF). This package is old by weight, ot volume. Some settings of contents may have occurred during shipping and handling.

Inactive ingredients

none

Tamper-Evident Disclosure

Do not use if the printed over-wrap over the bottle cap is torn, broken, or missing.

Principal Display Panel

Package Label 4 oz

Package Label 8 oz

Package Label 16 oz

INGREDIENTS AND APPEARANCE

D-D SUDIUM BICARBONATE U.S.P.  BICARBONATO DE SODA PURO
sodium bicarbonate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84178-105
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37, BICARBONATE ION - UNII:HN1ZRA3Q20)	SODIUM BICARBONATE	315 mg  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84178-105-02	113 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2026
2	NDC: 84178-105-03	227 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2026
3	NDC: 84178-105-04	454 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	01/14/2026

Labeler - Evi Labs (123617598)

Establishment
Name	Address	ID/FEI	Business Operations
Evi Labs		123617598	manufacture(84178-105)