DE LA CRUZ SODIUM BICARBONATE ANTACID

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: DE LA CRUZ SODIUM BICARBONATE ANTACID
Generic name: SODIUM BICARBONATE
Manufacturer: DLC Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: fc469943-9749-45ee-93f7-90fdbcdc7215
SPL ID: 47d4f7e8-3e03-1192-e063-6294a90aa739
Version: 10
Effective date: 2026-01-07
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:46:48

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		DE LA CRUZ SODIUM BICARBONATE ANTACID	openfda.brand_name
generic name		SODIUM BICARBONATE	openfda.generic_name
manufacturer name		DLC Laboratories, Inc.	openfda.manufacturer_name
ndc	package	24286-1537-8	openfda.package_ndc
ndc	package	24286-1537-7	openfda.package_ndc
ndc	product	24286-1537	openfda.product_ndc
ndc11	package	24286153708	derived:openfda.package_ndc
ndc11	package	24286153707	derived:openfda.package_ndc
rxcui		1488624	openfda.rxcui
spl id		47d4f7e8-3e03-1192-e063-6294a90aa739	id
spl set id		fc469943-9749-45ee-93f7-90fdbcdc7215	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 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. Do not use in children under 12 years of age. Ask a doctor before use if you have a sodium-restricted diet. Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. Stop use and ask a doctor if you have used the maximum dosage for 2 weeks severe stomach pain occurs after using this product If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children . In case of overdose get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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