Humco Sodium Bicarbonate

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Humco Sodium Bicarbonate
Generic name: SODIUM BICARBONATE
Manufacturer: Humco Holding Group, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: aeaa34f6-216d-49f3-8393-c7bda96a3e32
SPL ID: 52ba1edd-fc9b-bb47-e063-6394a90ad9b5
Version: 7
Effective date: 2026-05-26
Source export date: 2026-11-06
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/2233cb6af8c6b55a5e4a05449e8db0d2f259f3c061d5d001b654a8bea1cc1db2/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:53:40

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		Humco Sodium Bicarbonate	openfda.brand_name
generic name		SODIUM BICARBONATE	openfda.generic_name
manufacturer name		Humco Holding Group, Inc.	openfda.manufacturer_name
ndc	package	0395-2685-94	openfda.package_ndc
ndc	package	0395-2685-01	openfda.package_ndc
ndc	product	0395-2685	openfda.product_ndc
ndc11	package	00395268594	derived:openfda.package_ndc
ndc11	package	00395268501	derived:openfda.package_ndc
rxcui		1110802	openfda.rxcui
spl id		52ba1edd-fc9b-bb47-e063-6394a90ad9b5	id
spl set id		aeaa34f6-216d-49f3-8393-c7bda96a3e32	set_id
unii		8MDF5V39QO	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings FOR ORAL USE ONLY Except under supervision of a doctor: Do not administer to children under 12 years of age. Do not take more than six, 1/2 tsp. per person up to 60 years old, or three 1/2 tsp. per person 60 years or older in a 24 hour period. STOMACH WARNING: TO AVOID SERIOUS INJURY, DO NOT TAKE UNTIL POWDER IS COMPLETELY DISSOLVED. IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FULL FROM FOOD OR DRINK. FOR ORAL USE ONLY Except under supervision of a doctor: Do not administer to children under 12 years of age. Do not take more than six, 1/2 tsp. per person up to 60 years old, or three 1/2 tsp. per person 60 years or older in a 24 hour period. STOMACH WARNING: TO AVOID SERIOUS INJURY, DO NOT TAKE UNTIL POWDER IS COMPLETELY DISSOLVED. IT IS VERY IMPORTANT NOT TO TAKE THIS PRODUCT WHEN OVERLY FULL FROM FOOD OR DRINK.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.