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 32 of 34 · 678 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Premier Value Milk of Magnesia	MAGNESIUM HYDROXIDE	Pharmacy Value Alliance, LLC	c3cdaa2b-db34-872d-e053-2995a90a3826	2023-12-20	Warnings	Exact identifier application number: M001
Calcium Carbonate	CALCIUM CARBONATE	Humco Holding Group, Inc.	8b207b49-d3fd-4108-b611-dca27c9dc78a	2023-12-15	Warnings	Exact identifier application number: M001
Humco Dewees Carminative	MAGNESIUM CARBONATE	Humco Holding Group, inc.	163bceeb-ca74-413e-88b9-5c7bc9bbeb0d	2023-12-15	Warnings	Exact identifier application number: M001
Humco Milk of Magnesia	MAGNESIUM HYDROXIDE	Humco Holding Group, Inc.	b6c90fb4-2673-7e29-e053-2995a90ae9e1	2023-12-15	Warnings	Exact identifier application number: M001
Medis Sodium Bicarbonate	SODIUM BICARBONATE	Humco Holding Group, Inc	5da32469-58fc-14b1-e053-2a91aa0a74c4	2023-12-15	Warnings	Exact identifier application number: M001
Mylanta One Antacid/Anti-Gas	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, DIMETHICONE	Infirst Healthcare Inc.	aa694e0d-7891-4870-8106-dd57f1e29fb4	2023-12-11	Warnings	Exact identifier application number: M001
Mylanta One Antacid/Anti-Gas	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, DIMETHICONE	Infirst Healthcare Inc.	ed1b03f0-fabc-4c1c-8e6d-9f15c380300c	2023-12-11	Warnings	Exact identifier application number: M001
Sodium Bicarbonate Antacid	SODIUM BICARBONATE	Rugby Laboratories	e73b5871-4a87-4473-ab00-5e5395be017d	2023-12-06	Warnings	Exact identifier application number: M001
Inon Ace	MAGNESIUM ALUMINOSILICATE, MAGNESIUM HYDROXIDE	Sato Pharmaceutical Co., Ltd.	a6e4475c-dfac-493c-b98a-21473e3b59d5	2023-12-06	Warnings	Exact identifier application number: M001
INON	ALUMINUM HYDROXIDE, MAGNESIUM CARBONATE, SODIUM BICARBONATE	Sato Pharmaceutical Co., Ltd.	e86d9c57-c877-49f1-a405-95a9a226ccf3	2023-12-04	Warnings	Exact identifier application number: M001
Aluminum hydroxide and Magnesium carbonate	ALUMINUM HYDROXIDE, MAGNESIUM CARBONATE	Simpex Pharma Pvt. Ltd	e799a555-bfd0-4298-a5dc-aeb671815d40	2023-11-29	Warnings	Exact identifier application number: M001
Inon Ace	MAGNESIUM ALUMINOSILICATES, MAGNESIUM HYDROXIDE, SIMETHICONE	Sato Pharmaceutical Co., Ltd.	0af4355f-e160-409d-8471-2de98dbc6f7c	2023-11-10	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	STRATEGIC SOURCING SERVICES LLC	fd00ead8-026c-6610-e053-6394a90a0f11	2023-11-08	Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID AND ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	STRATEGIC SOURCING SERVICES LLC	fd67566a-1078-019d-e053-6394a90a415c	2023-11-08	Warnings	Exact identifier application number: M001
MAXIMUM STRENGTH ANTACID AND ANTIGAS	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	STRATEGIC SOURCING SERVICES LLC	fd7a0a90-6570-c722-e053-6394a90a03f4	2023-11-08	Warnings	Exact identifier application number: M001
GERI-LANTA SUPREME CHERRY	CALCIUM CARBONATE, MAGNESIUM HYDROXIDE	Geri-Care Pharmaceuticals, Corp	7fbc654b-a0d4-408c-bb5a-eb50b7b54382	2023-11-08	Warnings	Exact identifier application number: M001
ANTACID ANTIGAS NTA	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	AMERISOURCEBERGEN DRUG CORPORATION	5d6916ec-e87f-6421-e053-2991aa0a3364	2023-11-07	Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	AMERISOURCEBERGEN DRUG CORPORATION	5d68366d-fee9-2acf-e053-2991aa0a7e4b	2023-11-07	Warnings	Exact identifier application number: M001
ANTACID ANTIGAS NTA	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE	AMERISOURCEBERGEN DRUG CORPORATION	5d7ed0c5-911c-299a-e053-2a91aa0aae56	2023-11-07	Warnings	Exact identifier application number: M001
REGULAR STRENGTH ANTACID	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	AMERISOURCEBERGEN DRUG CORPORATION	5e1eed65-0d4c-2d02-e053-2991aa0a95c1	2023-11-07	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