Uline Antacid

Product NDC: 69790-089
Requested package NDC: 69790-089-33
11-digit product format: 697900089
Labeler code: 69790
Product ID: 69790-089_debc3184-6bb1-11d1-e053-2995a90af277
Type: HUMAN OTC DRUG
Nonproprietary name: calcium carbonate
Dosage form: TABLET, CHEWABLE
Route: ORAL
Labeler: Uline
Application: part331
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-10-07
Marketing end: 0000-00-00
Substance: CALCIUM CARBONATE
Active strength: 420 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: 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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	69790-089	69790-089-33	D	Discontinued by firm		2026-08-17

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99	Product name	1	20250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767	Product name	4	20250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2	Product name	5	20250304
334fe8d2-68fb-4331-a576-420e302ec069	Product name	7	20240320
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
e92765c1-be81-432a-b909-1b10777ec378	Product name	1	20190208
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
0441a8f5-3835-497c-aedd-bc78cba56b2a	Product name	1	20150317
87711080-88eb-65c5-b2dd-bf99e700a372	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69790-089-33	2023-08-31	C162847	48780-1	0191ceaa-6cbb-198a-e063-dbdaa90aec3e	Uline Antacid
69790-089-33	2023-07-28	C162847	48780-1	0191ceaa-6cbb-198a-e063-dbdaa90aec3e	Uline Antacid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69790-089-33	Uline Antacid	2 in 1 PACKET	TABLET, CHEWABLE	2		9
69790-089-33	Uline Antacid	50 in 1 BOX	TABLET, CHEWABLE	50		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69790-089	ULINE ANTACID (CALCIUM CARBONATE) TABLET, CHEWABLE [ULINE]	8	Legacy NDC, 2 package rows	20240127_9014f295-e816-9bcd-e053-2a95a90ae103.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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Uline Antacid	CALCIUM CARBONATE	Uline	9014f295-e816-9bcd-e053-2a95a90ae103	2025-09-08	Warnings	Exact identifier ndc (package): 69790-089-33 ndc (product): 69790-089 ndc11 (package): 69790008933

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
H0G9379FGK	CALCIUM CARBONATE	471-34-1	CALCIUM CARBONATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
313884	calcium carbonate 420 MG (Ca 168 MG) Chewable Tablet	PSN	9014f295-e816-9bcd-e053-2a95a90ae103	9
313884	calcium carbonate 420 MG Chewable Tablet	SCD	9014f295-e816-9bcd-e053-2a95a90ae103	9
313884	calcium carbonate 420 MG (calcium 168 MG) Chewable Tablet	SY	9014f295-e816-9bcd-e053-2a95a90ae103	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69790-089-33	69790008933	50 PACKET in 1 BOX (69790-089-33) > 2 TABLET, CHEWABLE in 1 PACKET	50 packet	2019-10-07	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Uline Antacid	Uline \| Unifirst First Aid Corporation \| Prestige Packaging \| Medique Products	2025-09-08	HUMAN OTC DRUG LABEL	9