FDA.reportPublic FDA data

DE LA CRUZ SODIUM BICARBONATE ANTACID

Manufacturer
DLC Laboratories, Inc.
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:31:53

Label at a glance#

ProductDE LA CRUZ SODIUM BICARBONATE ANTACID
Active ingredientSODIUM BICARBONATE
Label structure11 sections

Indications and uses

relieves: heartburn sour stomach acid indigestion upset stomach associated with these symptoms

Dosage and administration

take ½ level teaspoon in ½ glass (4 fl. oz.) of water every 2 hours up to maximum dosage or as directed by a doctor. Dissolve completely in water before drinking. Age Maximum Dosage Adults 60 years and over Do not exceed three doses of 1/2 teaspoon in a 24 hour period. Adults and children 12 years and over Do not exceed six doses of 1/2 teaspoon in a 24 hour period. Children under 12 years Do not use. Do not excee...

Storage and handling

each 1/2 teaspoon dose contains: sodium 716 mg

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each dose = 1/2 teaspoon)

OTC - ACTIVE INGREDIENT SECTION

Sodium bicarbonate USP 2,616 mg

Purpose

OTC - PURPOSE SECTION

Antacid

Uses

INDICATIONS & USAGE SECTION

relieves:

  • heartburn
  • sour stomach
  • acid indigestion
  • upset stomach associated with these symptoms

Warnings

WARNINGS SECTION

FOR ORAL USE ONLY

STOMACH WARNING

SPL UNCLASSIFIED SECTION

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.

OTC - DO NOT USE SECTION

Do not use in children under 12 years of age.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • a sodium-restricted diet.

OTC - ASK DOCTOR/PHARMACIST SECTION

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

OTC - STOP USE SECTION

  • you have used the maximum dosage for 2 weeks
  • severe stomach pain occurs after using this product

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take ½ level teaspoon in ½ glass (4 fl. oz.) of water every 2 hours up to maximum dosage or as directed by a doctor. Dissolve completely in water before drinking.
AgeMaximum Dosage
Adults 60 years and overDo not exceed three doses of 1/2 teaspoon in a 24 hour period.
Adults and children 12 years and overDo not exceed six doses of 1/2 teaspoon in a 24 hour period.
Children under 12 yearsDo not use.

Do not exceed recommended dosage. See warnings.

Other information

STORAGE AND HANDLING SECTION

  • each 1/2 teaspoon dose contains: sodium 716 mg

SPL UNCLASSIFIED SECTION

Distributed by:
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA

Questions

OTC - QUESTIONS SECTION

1-800-858-3889

Inactive Ingredient

INACTIVE INGREDIENT SECTION

none

PRINCIPAL DISPLAY PANEL - 113 g Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

De La Cruz ®

OVER
40
DOSES

Sodium
Bicarbonate

USP
- Oral Powder -

SUGAR
FREE

Antacid

NET WT 4 OZ (113g)

PRINCIPAL DISPLAY PANEL - 113 g Bottle Label
PRINCIPAL DISPLAY PANEL - 113 g Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1488624sodium bicarbonate 2.6 GM Powder for Oral SolutionPSN10
1488624sodium bicarbonate 2600 MG Powder for Oral SolutionSCD10
1488624NaHCO3 2600 MG Powder for Oral SolutionSY10
1488624sodium bicarbonate 2.6 GM Powder for Oral SolutionSY10

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BICARBONATE ION Pharmacologic Class Indexing1Indexing - Pharmacologic Class20220121

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24286-1537-7DE LA CRUZ SODIUM BICARBONATE ANTACID113 g in 1 BOTTLE, PLASTICPOWDER11310
24286-1537-8DE LA CRUZ SODIUM BICARBONATE ANTACID226 g in 1 BOTTLE, PLASTICPOWDER22610

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM BICARBONATEACTIVE INGREDIENT8MDF5V39QO4
BICARBONATE IONACTIVE MOIETYHN1ZRA3Q204

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24286-153724286-1537-7, 24286-1537-8

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM BICARBONATE8MDF5V39QOACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DE LA CRUZ SODIUM BICARBONATE ANTACIDSODIUM BICARBONATEDLC Laboratories, Inc.fc469943-9749-45ee-93f7-90fdbcdc72152026-01-07WarningsExact identifier
ndc (package): 24286-1537-8
ndc (package): 24286-1537-7
ndc (product): 24286-1537
ndc11 (package): 24286153708
ndc11 (package): 24286153707
spl id: 47d4f7e8-3e03-1192-e063-6294a90aa739
spl set id: fc469943-9749-45ee-93f7-90fdbcdc7215

Reported adverse events (FAERS/openFDA)#

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