Calcium Carbonate

Product NDC: 17856-3117
11-digit product format: 178563117
Labeler code: 17856
Product ID: 17856-3117_34f3682a-e5bc-851a-e063-6394a90a8e96
Type: HUMAN OTC DRUG
Nonproprietary name: Calcium Carbonate
Dosage form: SUSPENSION
Route: ORAL
Labeler: Atlantic Biologicals Corps
Application: M001
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2004-12-01
Substance: CALCIUM CARBONATE
Active strength: 1250 mg/5mL
Pharmacologic classes: Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 22 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	17856-3117-3	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	17856-3117-3	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	17856-3117-3	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	17856-3117-3	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	17856-3117-3	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	17856-3117-3	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	17856-3117-3	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	17856-3117-3	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	17856-3117-3	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	17856-3117-3	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	17856-3117-3	`1332a3947898…`	`d4bfe170f9cd…`

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: Calcium Carbonate
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CALCIUM CARBONATE	1250 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
H0G9379FGK	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
308891	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
38654d22-2f8a-49d2-a1cd-06d341f11323	Available on FDA.report

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
17856-3117-3	2025-03-18	C162847	48780-1	f386c64a-2f2b-0266-e053-dadaa90a7c1a	Calcium Carbonate
17856-3117-3	2023-01-30	C162847	48780-1	f386c64a-2f2b-0266-e053-dadaa90a7c1a	Calcium Carbonate

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
17856-3117-3	Calcium Carbonate	5 mL in 1 CUP	SUSPENSION	5		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17856-3117	CALCIUM CARBONATE SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	7	Current NDC, Legacy NDC, 1 package rows	20250514_38654d22-2f8a-49d2-a1cd-06d341f11323.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 34 of 34 · 678 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
REGULAR STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	VALU MERCHANDISERS COMPANY	5e82a4f4-c7da-09cb-e053-2a91aa0abf5b	2023-11-01	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	WAL-MART STORES, INC.	7cc2ad32-fdff-0772-e053-2a91aa0aad9e	2023-11-01	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID CHERRY	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	WAL-MART STORES, INC.	7cc2771e-abd7-4120-e053-2a91aa0a8af0	2023-11-01	Warnings	Exact identifier application number: M001
MINTOX MAXIMUM STRENGTH	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	Proficient Rx LP	b7711b50-c14a-44d6-b647-1f31284f87ea	2023-11-01	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID AND ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	VALU MERCHANDISERS COMPANY	5e811783-cbf6-d0e3-e053-2991aa0ae69f	2023-10-31	Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	CVS	5f880b43-2977-7a2d-e053-2991aa0a024d	2023-10-31	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	CVS PHARMACY	d5661964-9d2c-7a3d-e053-2995a90a86ef	2023-10-31	Warnings	Exact identifier application number: M001
EXTRA STRENGTH HEARTBURN RELIEF	ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE	CVS PHARMACY,INC.	53fc327e-e345-26f2-e054-00144ff8d46c	2023-10-31	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID AND ANTIGAS CHERRY	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	VALU MERCHANDISERS COMPANY	5e94cb90-b616-dcfe-e053-2a91aa0ada72	2023-10-31	Warnings	Exact identifier application number: M001
CALCIUM CARBONATE CHEWABLE ANTACID	CALCIUM CARBONATE	Geri-Care Pharmaceutical Corp	27d9b505-08bd-4261-a59d-6ddc4031be32	2023-10-25	Warnings	Exact identifier application number: M001
CALCIUM CARBONATE	CALCIUM CARBONATE	Blessings International	99d7e467-a3db-b4f0-e053-2a95a90a900f	2023-10-25	Warnings	Exact identifier application number: M001
Sodium Bicarbonate	SODIUM BICARBONATE	APNAR PHARMA LP	e206c240-55c2-2d00-e053-2a95a90a1779	2023-10-21	Boxed warning, Warnings	Exact identifier application number: M001
Magnesium Oxide	MAGNESIUM OXIDE	APNAR PHARMA LP	e4ef2224-07e4-e913-e053-2995a90a28ed	2023-10-21	Warnings	Exact identifier application number: M001
Magnesium Oxide	MAGNESIUM OXIDE	Endo USA	d5c123f8-1396-4d8c-96d3-e5ade96a6ef8	2020-11-10	Warnings	Exact identifier application number: M001
Magnesium Oxide	MAGNESIUM OXIDE	Endo USA	d3c5b01b-f0d6-4503-ab18-b1a72386e2c6	2020-06-03	Warnings	Exact identifier application number: M001
Magnesium Oxide 400mg	MAGNESIUM OXIDE 400MG	Allegiant Health	2ea68874-8c20-4284-bd0a-f07768057b83	2019-01-28	Warnings	Exact identifier application number: M001
Calcium Antacid	CALCIUM CARBONATE	Allegiant Health	51dd53e8-22ff-4967-9124-f15c3986e4dd	2017-11-17	Warnings	Exact identifier application number: M001
Calcium Antacid	CALCIUM CARBONATE	Allegiant Health	551d6135-2650-4c27-a20d-d56a9aba7b71	2017-11-08	Warnings	Exact identifier application number: M001

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
308891	calcium carbonate 1250 MG in 5 mL Oral Suspension	PSN	38654d22-2f8a-49d2-a1cd-06d341f11323	7
308891	calcium carbonate 250 MG/ML Oral Suspension	SCD	38654d22-2f8a-49d2-a1cd-06d341f11323	7
308891	calcium carbonate 1250 MG (calcium 500 MG) per 5 ML Oral Suspension	SY	38654d22-2f8a-49d2-a1cd-06d341f11323	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17856-3117-3	17856311703	5 mL in 1 CUP (17856-3117-3)	5 ml	2021-01-28	0000-00-00	No	No	Current