Home NDC 0395-2685 Humco Sodium Bicarbonate
Product NDC 0395-2685
11-digit product format 003952685
Labeler code 0395
Product ID 0395-2685_52ba1edd-fc9b-bb47-e063-6394a90ad9b5
Type HUMAN OTC DRUG
Nonproprietary name Sodium Bicarbonate
Dosage form POWDER
Route ORAL
Labeler Humco Holding Group, Inc.
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 1998-03-25
Substance SODIUM BICARBONATE
Active strength 1000 mg/g
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 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 Humco Sodium Bicarbonate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM BICARBONATE 1000 mg/g
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 1110802 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0395-2685-01 Humco Sodium Bicarbonate 454 g in 1 BOTTLE, PLASTIC POWDER 454 7 0395-2685-94 Humco Sodium Bicarbonate 113 g in 1 BOTTLE, PLASTIC POWDER 113 7
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0395-2685 HUMCO SODIUM BICARBONATE (SODIUM BICARBONATE) POWDER [HUMCO HOLDING GROUP, INC.] 5 Current NDC, Legacy NDC, 2 package rows 20231216_aeaa34f6-216d-49f3-8393-c7bda96a3e32.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 0395-2685-01 00395268501 454 g in 1 BOTTLE, PLASTIC (0395-2685-01) 454 g 2017-11-14 0000-00-00 No No Current 0395-2685-94 00395268594 113 g in 1 BOTTLE, PLASTIC (0395-2685-94) 113 g 2017-11-14 0000-00-00 No No Current