Home FDA labels 5195cab5-bddb-2ddf-e063-6394a90ac9fe Sodium Bicarbonate openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Sodium Bicarbonate
Generic name SODIUM BICARBONATE
Manufacturer Vitamex USA, Corp
Product type HUMAN OTC DRUG
SPL set ID 5195cab5-bdda-2ddf-e063-6394a90ac9fe
SPL ID 5195cab5-bddb-2ddf-e063-6394a90ac9fe
Version 1
Effective date 2026-05-11
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:07:53 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 11 matching rows.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings Warnings: • For Oral use Only. • To avoid serious injuries. • Do not take until powder is completely dissolved. • It is very important not to take this product when overly full from food or drink. • Ask a doctor before use if: - You have a sodium restricted diet. - If you are presently taking a prescription.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.