Alka-Seltzer Ultra Strength Heartburn ReliefChews

Manufacturer
Bayer HealthCare LLC.
Effective date
2025-12-04
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:19:56

Label at a glance#

ProductAlka-Seltzer Ultra Strength Heartburn ReliefChews Strawberry and Orange
Active ingredientCALCIUM CARBONATE
Label structure10 sections

Indications and uses

Uses for the relief of: ● acid indigestion ● heartburn ● sour stomach ● upset stomach associated with these symptoms

Dosage and administration

Directions ● adults and children 12 years and over: fully chew then swallow 2 to 3 chewable tablets as symptoms occur, or as directed by a doctor ● children under 12 years: consult a doctor ● do not take more than 5 chewable tablets in a 24-hour period ● if pregnant, do not take more than 5 chewable tablets in 24 hours

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each chewable tablet)

Calcium carbonate 1000 mg

OTC - PURPOSE SECTION

Purpose

Antacid

Uses

INDICATIONS & USAGE SECTION

Uses for the relief of:

● acid indigestion ● heartburn ● sour stomach

● upset stomach associated with these symptoms

WARNINGS SECTION

Warnings
Do not use if you have ever had an allergic reaction to this product or any of its ingredients

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.

OTC - WHEN USING SECTION

When using this product
● do not take more than 5 chewable tablets in a 24-hour
period

● if pregnant do not take more than 5 chewable tablets in 24

hours

● do not use the maximum dosage of this product for more

than 2 weeks except under the advice and supervision of a

physician

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, inform your doctor that you are using this product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

● adults and children 12 years and over: fully chew then swallow 2 to 3 chewable tablets as symptoms occur, or as directed by a doctor

● children under 12 years: consult a doctor

● do not take more than 5 chewable tablets in a 24-hour period

● if pregnant, do not take more than 5 chewable tablets in 24

hours

OTHER SAFETY INFORMATION

Other information

● each chewable tablet contains: calcium 400 mg

● store at room temperature. Avoid excessive heat above 40°C

(104°F).

● close cap tightly after use

INACTIVE INGREDIENT SECTION

Inactive ingredients acacia, carnauba wax, citric acid, corn syrup, dextrin, FD&C Blue #1 aluminum lake, FD&C Red #40 aluminum lake, FD&C Yellow #6, FD&C Yellow #6 aluminum lake, flavors, hydrogenated coconut oil, lecithin, maltodextrin, medium-chain triglycerides, methylparaben, phosphoric acid, polyvinylpyrrolidone, propylene glycol, propylparaben, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, sucrose, titanium dioxide, vegetable oil, white wax

Questions or comments

OTC - QUESTIONS SECTION

Questions or comments? 1-800-986-0369

(Mon – Fri 9AM – 5PM EST)

50 Tablet bottle label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW!

Delicious

Creme

Flavors

Starts Neutralizing Acid

in Seconds!

Alka-Seltzer®

Calcium Carbonate/Antacid

ULTRA STRENGTH

HEARTBURN

RELIEFCHEWS®

Strawberry &

Orange Creme

50 CHEWABLE TABELTS

Bottle label 50 countBottle label 50 count

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308892calcium carbonate 1000 MG (Ca 400 MG) Chewable TabletPSN6
308892calcium carbonate 1000 MG Chewable TabletSCD6
308892calcium carbonate 1000 MG (calcium 400 MG) Chewable TabletSY6

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0280-0059-50Alka-Seltzer Ultra Strength Heartburn ReliefChewsStrawberry and Orange50 in 1 BOTTLE, PLASTICTABLET, CHEWABLE506

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0280-00590280-0059-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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
Alka-Seltzer Ultra Strength Heartburn ReliefChews Strawberry and OrangeCALCIUM CARBONATEBayer HealthCare LLC.84771ac5-ad0b-e0ec-e053-2a91aa0a1b362025-12-04WarningsExact identifier
ndc (package): 0280-0059-50
ndc (product): 0280-0059
ndc11 (package): 00280005950
spl id: 45262db7-ea04-6c50-e063-6394a90a025d
spl set id: 84771ac5-ad0b-e0ec-e053-2a91aa0a1b36

Reported adverse events (FAERS/openFDA)#

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