Home NDC 69469-100 Sodium Bicarbonate
Product NDC 69469-100
11-digit product format 694690100
Labeler code 69469
Product ID 69469-100_5195cab5-bddb-2ddf-e063-6394a90ac9fe
Type HUMAN OTC DRUG
Nonproprietary name Sodium Bicarbonate
Dosage form POWDER
Route ORAL
Labeler Vitamex USA, Corp
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-01
Substance SODIUM BICARBONATE
Active strength 2.6 g/2.6g
Pharmacologic classes Alkalinizing Activity [MoA]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Sodium Bicarbonate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 2.6 g/2.6g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8MDF5V39QO Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1488624 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 8 of 34 · 678 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 69469-100-04 69469010004 113 g in 1 BOTTLE, PLASTIC (69469-100-04) 113 g 2026-05-01 No No Current