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 28 of 36 · 719 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Magnesium Oxide MAGNESIUM OXIDE Richmond Pharmaceuticals, Inc. db5941b2-0a04-452a-8fbc-bd5e40fadfb1 2024-12-26 Warnings Exact identifier application number: M001 Bi-Mart Ultra Strength Antacid Assorted Fruit CALCIUM CARBONATE Bi-Mart 662c1a29-ab47-49d5-97ad-dc55f4cda591 2024-12-26 Warnings Exact identifier application number: M001 Bi-Mart Extra Strength Antacid Assorted Fruit CALCIUM CARBONATE Bi-Mart da70ba03-ed38-4fce-939e-04c7eec06087 2024-12-26 Warnings Exact identifier application number: M001 HEB Extra Strength Smooth Antacid Assorted Fruits CALCIUM CARBONATE H E B 2faac316-7b59-4df8-b751-37069e865263 2024-12-26 Warnings Exact identifier application number: M001 Good Neighbor Pharmacy Antacid Extra Strength CALCIUM CARBONATE AmerisourceBergen Drug Corporation 5e3a3c20-dabe-4427-9e75-99759905caa0 2024-12-26 Warnings Exact identifier application number: M001 BI-MART Regular Strength Antacid CALCIUM CARBONATE Bi-Mart 19afcf54-2090-4588-9af8-e6536db8fda0 2024-12-26 Warnings Exact identifier application number: M001 BI-MART Regular Strength Antacid Peppermint CALCIUM CARBONATE Bi-Mart 26580067-050a-489d-bcfa-14cf8eebf892 2024-12-26 Warnings Exact identifier application number: M001 Maximum Strength Antacid Cherry liquid ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE Topco Associates, LLC 31d2e77d-5eda-4f47-917c-3390d6c782af 2024-12-26 Warnings Exact identifier application number: M001 Maximum Strength Antacid Mint ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE Topco Associates, LLC 50ceff1e-b6df-40f8-89f3-667cc8f9e750 2024-12-26 Warnings Exact identifier application number: M001 HEB Extra Strength Smooth Antacid Peppermint CALCIUM CARBONATE H E B d04e691e-6d1c-4c39-9504-7ac0f1bd197d 2024-12-26 Warnings Exact identifier application number: M001 Antacid ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE H E B f294cf44-fb21-4b2e-8b7c-efd41416c6b2 2024-12-26 Warnings Exact identifier application number: M001 Antacid CALCIUM CARBONATE Trifecta Pharmaceuticals USA LLC 14a7916e-5363-7f1b-e063-6294a90a20aa 2024-12-20 Warnings Exact identifier application number: M001 maximum strength antacid cherry ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE UNITED NATURAL FOODS, INC. DBA UNFI d6b49f0a-cf05-4b1b-8cad-c5795aa31645 2024-12-20 Warnings Exact identifier application number: M001 GOODSENSE Ultra Strength Antacid Peppermint CALCIUM CARBONATE GoodSense 04950b56-7760-4b6c-8110-86b6a3f795b4 2024-12-19 Warnings Exact identifier application number: M001 Goodsense Regular Strength Antacid Peppermint CALCIUM CARBONATE GoodSense 32c04f3e-59f3-44aa-ad92-672444982710 2024-12-19 Warnings Exact identifier application number: M001 GOODSENSE Ultra Strength Antacid Assorted Fruit CALCIUM CARBONATE GoodSense ad4d51f6-b55b-45db-b034-fb3da54fbe99 2024-12-19 Warnings Exact identifier application number: M001 TUMS Extra Strength Sugar-Free CALCIUM CARBONATE Haleon US Holdings LLC 3495102f-55d2-4a94-8d55-f46f49e00c27 2024-12-19 Warnings Exact identifier application number: M001 Goodsense Extra Strength Antacid Assorted Fruit CALCIUM CARBONATE GoodSense ae6270fc-0f8d-4bba-8f12-adba3f07f7c5 2024-12-19 Warnings Exact identifier application number: M001 Quality Choice Extra Strength Assorted Berry Antacid Extra strength Assorted Berry Antacid CALCIUM CARBONATE Chain Drug Marketing Association Inc. ec729051-72d3-4d1a-8e39-d4495d5c1cf3 2024-12-18 Warnings Exact identifier application number: M001 Guardian Extra Strength Antacid CALCIUM CARBONATE Guardian Drug Company aef3d830-c5c3-4f72-86ba-d31945a756db 2024-12-18 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