Vida Mia Sodium Bicarbonate

Manufacturer
Navarro Discount Pharmacies, LLC | Humco Holding Group, Inc.
Effective date
2018-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:47:29

Label at a glance#

ProductVida Mia Sodium Bicarbonate
Active ingredientSODIUM BICARBONATE
Label structure10 sections

Dosage and administration

Adult and children 6 yrs of age and older: Take 1/2 tsp. in 1/2 g;ass (4 fl oz) of water every 2 hrs. up to maximum dosage or as directed by doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION


Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Soduim Bicarbonate, USP

Purpose

OTC - PURPOSE SECTION

Antacid

Use

INDICATIONS & USAGE SECTION

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

Warnings NOT FOR INJECTIONS

WARNINGS SECTION

Except under supervision of a doctor do not administer to children under 6 years of age.

Do not take more than six, 1/2 tsp. per person up to 60 years old, or three 1/2 tsp. per person 60 years or older in a 24 hour period.

Do not use this product if you are on a sodium restricted diet (each 1/2 tsp. contains 30 mEq (0.7 g) Sodium).

Do not use the maximum does more than 2 weeks.

Ask a doctor or pharmacist before use if

OTC - ASK DOCTOR/PHARMACIST SECTION

you are currently taking a prescription drug. Antacids may interact with certain prescription drugs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adult and children 6 yrs of age and older:

Take 1/2 tsp. in 1/2 g;ass (4 fl oz) of water every 2 hrs. up to maximum dosage or as directed by doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

none

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59970-68559970-685-01, 59970-685-94

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM BICARBONATE8MDF5V39QOACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b6d97c0b-6db2-28db-e053-2a95a90ace7b5d91fc56-a560-d003-e053-2a91aa0a20622020-12-19WarningsExact identifier
spl set id: 5d91fc56-a560-d003-e053-2a91aa0a2062

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.