Home NDC 69618-034 Sodium Bicarbonate 10 gr
Product NDC 69618-034
11-digit product format 696180034
Labeler code 69618
Product ID 69618-034_2bc8028b-eebb-902f-e063-6394a90a382b
Type HUMAN OTC DRUG
Nonproprietary name Sodium Bicarbonate
Dosage form TABLET, SOLUBLE
Route ORAL
Labeler Reliable 1 Laboratories LLC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-11-01
Substance SODIUM BICARBONATE
Active strength 648 mg/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 69618-034-10 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 69618-034-10 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 69618-034-10 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 69618-034-10 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 69618-034-10 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 69618-034-10 1332a3947898…d4bfe170f9cd…
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 10 gr
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 648 mg/1
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 198861 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69618-034-10 Sodium Bicarbonate 10 gr 1000 in 1 BOTTLE, PLASTIC TABLET, SOLUBLE 1000 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69618-034 SODIUM BICARBONATE 10 GR (SODIUM BICARBONATE) TABLET, SOLUBLE [RELIABLE 1 LABORATORIES LLC] 6 Current NDC, Legacy NDC, 1 package rows 20250117_321a772c-c44c-3d4e-e054-00144ff8d46c.zip
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 17 of 36 · 719 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Extra Strength Antacid Calcium Carbonate,750 mg CALCIUM CARBONATE TARGET CORPORATION 07aa39bb-c409-ce4f-e063-6394a90a7069 2025-11-04 Warnings Exact identifier application number: M001 ADVANCED REGULAR STRENGTH ANTACID ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE WALGREEN COMPANY 5faf6229-b0fd-58df-e053-2a91aa0ab3bb 2025-10-30 Warnings Exact identifier application number: M001 Regular Strength Antacid CALCIUM CARBONATE SAFEWAY ce44254f-6e33-4cbd-a609-6a926376efaf 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength CALCIUM CARBONATE BETTER LIVING BRANDS, LLC 9b311b76-1892-4b74-a07a-8b321436d4a0 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength ANTACID TABLETS SAFEWAY f91aa7da-8bdc-4fd2-a9de-fef21674e515 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength Smooth CALCIUM CARBONATE SAFEWAY 4314ac58-03aa-479c-a711-4818cc332531 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength ANTACID TABLETS SAFEWAY 5bdb868d-016d-4175-9283-86c5b77bb26e 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength ANTACID TABLETS SAFEWAY 03853f03-081d-4a78-b383-66ac9754d46f 2025-10-29 Warnings Exact identifier application number: M001 Ultra Strength CALCIUM CARBONATE BETTER LIVING BRANDS LLC 3ff92c9a-987f-468e-9e18-1e3e171ede14 2025-10-29 Warnings Exact identifier application number: M001 Ultra Strength CALCIUM CARBONATE BETTER LIVING BRANDS LLC 35b3d9d0-b04d-4f6d-b99d-435233803d4b 2025-10-29 Warnings Exact identifier application number: M001 Ultra Strength ANTACID TABLETS SAFEWAY 4c6cdd81-5145-4a1f-888f-85cf5d856c39 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength Smooth ANTACID TABLETS SAFEWAY 8ed35c3b-9878-4889-90f7-a3973cf806e0 2025-10-29 Warnings Exact identifier application number: M001 Publix Regular Strength Assorted Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC fd637431-7a08-4454-9cae-a68716d2d0fa 2025-10-28 Warnings Exact identifier application number: M001 Publix Regular Strength Peppermint Flavor CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC c41b6cc2-c852-45fd-858c-c7bedc5dc882 2025-10-28 Warnings Exact identifier application number: M001 Publix Extra Strength Assorted Berry CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC a270fc36-f2b2-4f56-81d4-cf165f6b5abe 2025-10-28 Warnings Exact identifier application number: M001 Extra Strength Sugar Free Orange Cream Flavor CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 4dbdabc4-280d-4c9a-8c54-84afc615c8c7 2025-10-28 Warnings Exact identifier application number: M001 Publix Extra Strength Tropical Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 28e8dd03-25cf-43db-8c4d-3aae99be9d53 2025-10-28 Warnings Exact identifier application number: M001 Publix Ultra Strength Assorted Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 9e1c883f-016e-4c05-b27a-750d14c0f3e5 2025-10-28 Warnings Exact identifier application number: M001 Ultra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc., 48827658-02f7-4599-a90a-1543b30b9de1 2025-10-27 Warnings Exact identifier application number: M001 Regular Strength Antacid ANTACID Wal-Mart Stores,Inc., 6e7cd170-b169-4fc0-bc90-f4421bbd9fcd 2025-10-27 Warnings Exact identifier application number: M001
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69618-034-10 69618003410 1000 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (69618-034-10) 2015-11-01 0000-00-00 No No Current