Home NDC 70795-1190-2 Sodium Bicarbonate 10 gr
Product NDC 70795-1190
Requested package NDC 70795-1190-2
11-digit product format 707951190
Labeler code 70795
Product ID 70795-1190_46cfbf8a-0ee3-a51f-e063-6394a90a063c
Type HUMAN OTC DRUG
Nonproprietary name Sodium Bicarbonate
Dosage form TABLET
Route ORAL
Labeler GRAXCELL PHARMACEUTICAL, LLC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-10-02
Substance SODIUM BICARBONATE
Active strength 650 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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 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 650 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# NDC, Effective, Related label table NDC Effective Related label 70795-1190-0 2025-12-25 Sodium Bicarbonate 10 gr (650 mg), 70795-1190 70795-1190-1 2025-12-25 Sodium Bicarbonate 10 gr (650 mg), 70795-1190 70795-1190-2 2025-12-25 Sodium Bicarbonate 10 gr (650 mg), 70795-1190 70795-1190-5 2025-12-25 Sodium Bicarbonate 10 gr (650 mg), 70795-1190 70795-1190-0 2024-01-30 Sodium Bicarbonate 10 gr (650 mg), 70795-1190 70795-1190-1 2024-01-30 Sodium Bicarbonate 10 gr (650 mg), 70795-1190 70795-1190-2 2024-01-30 Sodium Bicarbonate 10 gr (650 mg), 70795-1190 70795-1190-5 2024-01-30 Sodium Bicarbonate 10 gr (650 mg), 70795-1190
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70795-1190-0 Sodium Bicarbonate 10 gr 1000 in 1 BOTTLE TABLET 1000 9 70795-1190-1 Sodium Bicarbonate 10 gr 100 in 1 BOTTLE TABLET 100 9 70795-1190-2 Sodium Bicarbonate 10 gr 200 in 1 BOTTLE TABLET 200 9 70795-1190-5 Sodium Bicarbonate 10 gr 500 in 1 BOTTLE TABLET 500 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70795-1190 SODIUM BICARBONATE 10 GR (SODIUM BICARBONATE) TABLET [GRAXCELL PHARMACEUTICAL, LLC] 7 Current NDC, Legacy NDC, 4 package rows 20211222_897dbb09-fb47-4e03-8cae-bf76d48a7a03.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 8 of 34 · 678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70795-1190-2 70795119002 200 TABLET in 1 BOTTLE (70795-1190-2) 200 tablet 2017-10-02 0000-00-00 No No Current