FDA.reportPublic FDA data

Ultra Strength Antacid

Product NDC
69842-171
11-digit product format
698420171
Labeler code
69842
Product ID
69842-171_ce8cfb77-e2d9-42a6-985c-534591993edb
Type
HUMAN OTC DRUG
Nonproprietary name
Calcium Antacid
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
CVS
Application
part331
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2011-12-09
Substance
CALCIUM CARBONATE
Active strength
1000 mg/1
Pharmacologic classes
Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Ultra Strength Antacid
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CALCIUM CARBONATE1000 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
H0G9379FGKInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
308892Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
51acc196-ab1f-49ea-8a59-f06309f1953bAvailable on FDA.report

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
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-171-68Ultra Strength Antacid72 in 1 BOTTLETABLET, CHEWABLE721
69842-171-72Ultra Strength Antacid160 in 1 BOTTLETABLET, CHEWABLE1601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-171ULTRA STRENGTH ANTACID (CALCIUM ANTACID) TABLET, CHEWABLE [CVS]1Current NDC, Legacy NDC, 2 package rows20170809_51acc196-ab1f-49ea-8a59-f06309f1953b.zip

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
Ultra Strength AntacidCALCIUM ANTACIDCVS51acc196-ab1f-49ea-8a59-f06309f1953b2017-08-09WarningsExact identifier
ndc (product): 69842-171

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308892calcium carbonate 1000 MG (Ca 400 MG) Chewable TabletPSN51acc196-ab1f-49ea-8a59-f06309f1953b1
308892calcium carbonate 1000 MG Chewable TabletSCD51acc196-ab1f-49ea-8a59-f06309f1953b1
308892calcium carbonate 1000 MG (calcium 400 MG) Chewable TabletSY51acc196-ab1f-49ea-8a59-f06309f1953b1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
69842-171-686984201716872 TABLET, CHEWABLE in 1 BOTTLE (69842-171-68) 2011-12-090000-00-00NoNoCurrent
69842-171-7269842017172160 TABLET, CHEWABLE in 1 BOTTLE (69842-171-72) 2011-12-090000-00-00NoNoCurrent