FDA.reportPublic FDA data

DGH Antacid Ultra Strength 1000 Berry assorted 72ct

Product NDC
71481-002
11-digit product format
714810002
Labeler code
71481
Product ID
71481-002_d952df94-4215-4b74-e053-2995a90afc29
Type
HUMAN OTC DRUG
Nonproprietary name
CALCIUM CARBONATE
Dosage form
TABLET
Route
ORAL
Labeler
BioV Health Inc
Application
part331
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2022-02-28
Marketing end
0000-00-00
Substance
CALCIUM CARBONATE
Active strength
1000 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71481-002IInactivated by FDA2026-10-16
excluded packagepackage71481-00271481-002-01IInactivated by FDA2026-10-16

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71481-002-01d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71481-002-01f5e01cc5f278…a2eaf40c39c3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage71481-002-011332a3947898…d4bfe170f9cd…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71481-002-012025-07-29C16284748780-11030e365-52f0-111a-e063-dadaa90a10e2DGH Antacid Ultra Strength 1000 Berry assorted
71481-002-012024-04-04C16284748780-11030e365-52f0-111a-e063-dadaa90a10e2DGH Antacid Ultra Strength 1000 Berry assorted
71481-002-012024-01-30C16284748780-11030e365-52f0-111a-e063-dadaa90a10e2DGH Antacid Ultra Strength 1000 Berry assorted

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71481-002-01DGH Antacid Ultra Strength 1000 Berry assorted 72ct72 in 1 BOTTLETABLET722

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71481-002DGH ANTACID ULTRA STRENGTH 1000 BERRY ASSORTED 72CT (CALCIUM CARBONATE) TABLET [BIOV HEALTH INC]2Legacy NDC, 1 package rows20240405_4c508f05-ac26-4bb9-af7f-704455b2d47c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
308892calcium carbonate 1000 MG (Ca 400 MG) Chewable TabletPSN4c508f05-ac26-4bb9-af7f-704455b2d47c2
308892calcium carbonate 1000 MG Chewable TabletSCD4c508f05-ac26-4bb9-af7f-704455b2d47c2
308892calcium carbonate 1000 MG (calcium 400 MG) Chewable TabletSY4c508f05-ac26-4bb9-af7f-704455b2d47c2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71481-002-017148100020172 TABLET in 1 BOTTLE (71481-002-01) 72 tablet2022-02-280000-00-00NoNoCurrent