Sodium Bicarbonate 10 gr

Manufacturer
Bryant Ranch Prepack
Effective date
2019-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:22:29

Label at a glance#

ProductSodium Bicarbonate 10 gr
Active ingredientSODIUM BICARBONATE
Label structure16 sections

Dosage and administration

do not use the maximum dosage for more than 2 weeks dissolve tablets completely in water prior to use adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tabelts in 24 hours adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Sodium bicarbonte 10 gr

Purpose

OTC - PURPOSE SECTION

Antacid

INDICATIONS & USAGE SECTION

Uses relieves

  • acid indigestion
  • heartburn
  • sour stomach
  • upset stomach associated with these symptoms

Warnings

WARNINGS SECTION

Ask a doctor before use if you have a sodium restricted diet

Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.

Stop use and ask a doctor if symptoms last more than 2 weeks

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have a sodium restricted diet

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms last more than 2 weeks

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not use the maximum dosage for more than 2 weeks
  • dissolve tablets completely in water prior to use
  • adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tabelts in 24 hours
  • adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose sodium, microcrystalline cellulose, stearic acid

Questions or comments?

OTC - QUESTIONS SECTION

call 516-341-0666, 8:30 am- 4:30 pm ET, Monday-Friday

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFTY SEAL UNDER CAP IS BROKEN OR MISSING

SPL UNCLASSIFIED SECTION

Distributed by: Reliable 1 Laboratories LLC

Valley Stream, NY 11580

www.reliable1labs.com

HOW SUPPLIED

HOW SUPPLIED SECTION

Product: 63629-7935

NDC: 63629-7935-1 30 TABLET in a BOTTLE

NDC: 63629-7935-2 90 TABLET in a BOTTLE

Sodium Bicarbonate 650mg (10gr) Tab

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Image
Label Image

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69618-034-10EA - Each69618-0348774e945-56f9-47f5-8fab-22387140da4312016-05-16

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63629-793563629-7935-1, 63629-7935-2
69618-034

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sodium Bicarbonate 10 grSODIUM BICARBONATEReliable 1 Laboratories LLC321a772c-c44c-3d4e-e054-00144ff8d46c2025-01-15WarningsExact identifier
ndc (product): 69618-034
c18dadf0-8963-414c-b7bd-4f79bd242010a9aa1499-b4c9-4dac-841b-aa8accfc7cf12020-12-28WarningsExact identifier
spl set id: a9aa1499-b4c9-4dac-841b-aa8accfc7cf1

Reported adverse events (FAERS/openFDA)#

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