De La Cruz Desempacho

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 Desempacho
Generic name: SODIUM BICARBONATE
Manufacturer: DLC LABORATORIES, INC.
Product type: HUMAN OTC DRUG
SPL set ID: 741e105a-3ed2-4fc7-ab06-273e515a2d16
SPL ID: 47d52ba7-4a48-9435-e063-6294a90ab2dd
Version: 14
Effective date: 2026-01-07
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:46

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M001	openfda.application_number
brand name		De La Cruz Desempacho	openfda.brand_name
generic name		SODIUM BICARBONATE	openfda.generic_name
manufacturer name		DLC LABORATORIES, INC.	openfda.manufacturer_name
ndc	package	24286-1523-4	openfda.package_ndc
ndc	product	24286-1523	openfda.product_ndc
ndc11	package	24286152304	derived:openfda.package_ndc
rxcui		1305099	openfda.rxcui
rxcui		1305093	openfda.rxcui
spl id		47d52ba7-4a48-9435-e063-6294a90ab2dd	id
spl set id		741e105a-3ed2-4fc7-ab06-273e515a2d16	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 Do not use this product when abdominal pain, nausea, vomiting or other symptoms of appendicitis are present if you have ever had an allergic reaction to this product or any of its ingredients 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. When using this product take only the recommended dosage do not use the maximum dosage for more than 2 weeks, unless directed by a doctor Stop use and ask a doctor if severe stomach pain occurs after taking this product. If pregnant or breast-feeding , 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.