GERI-LANTA ANTACID ANTIGAS

Product NDC: 17856-0630
11-digit product format: 178560630
Labeler code: 17856
Product ID: 17856-0630_34f47c5f-85f4-f00b-e063-6394a90a663e
Type: HUMAN OTC DRUG
Nonproprietary name: aluminum hydroxide, magnesium hydroxide, dimethicone
Dosage form: SUSPENSION
Route: ORAL
Labeler: ATLANTIC BIOLOGICALS CORP.
Application: M001
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2000-01-01
Substance: ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE
Active strength: 200; 200; 20 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classes: Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
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 · 10 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
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	17856-0630-1	`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	17856-0630-1	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	17856-0630-1	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	17856-0630-1	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	17856-0630-1	`bd6a592717d7…`	`303034d00443…`

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: GERI-LANTA ANTACID ANTIGAS
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALUMINUM HYDROXIDE	200 mg/5mL
MAGNESIUM HYDROXIDE	200 mg/5mL
DIMETHICONE	20 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5QB0T2IUN0	Internal UNII lookup
NBZ3QY004S	Internal UNII lookup
92RU3N3Y1O	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
307746	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
043207dd-5e1c-4c78-b75a-7d341d71b117	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6e3c022f-0786-43f1-8857-edff89d5153f	Product name	1	20260309
95250459-30e4-45c1-b08a-993044f49109	Product name	2	20250805
efd58652-cb8f-4018-91ca-4b0eb2ff729f	Product name	7	20240226
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
9badc7be-250a-44ab-aa36-926af3f02679	Product name	1	20210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62	Product name	3	20210309
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
26acd337-b838-40ac-bcbc-05c3b81c8712	Product name	1	20170323
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
e7e58cd3-cacb-49df-8d34-1ee335614abb	Product name	1	20150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
17856-0630-1	2024-05-24	C162847	48780-1	d6a99b39-8123-a426-e053-dadaa90af4c2	Geri-lanta original 629
17856-0630-1	2022-01-28	C162847	48780-1	d6a99b39-8123-a426-e053-dadaa90af4c2	Geri-lanta original 629

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
17856-0630-1	GERI-LANTA ANTACID ANTIGAS	50 in 1 BOX, UNIT-DOSE	SUSPENSION	50		6
17856-0630-1	GERI-LANTA ANTACID ANTIGAS	30 mL in 1 CUP, UNIT-DOSE	SUSPENSION	30		6

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
17856-0630-1	ML - Milliliter	17856-0630	996842c1-876a-428e-b266-a05db268c822	1	2024-04-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17856-0630	GERI-LANTA ANTACID ANTIGAS (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORP.]	6	Current NDC, Legacy NDC, 2 package rows	20250514_043207dd-5e1c-4c78-b75a-7d341d71b117.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 12 of 34 · 678 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Heartburn and gas fruit chews	CALCIUM CARBONATE	CVS Pharmacy	4a656a9f-8f34-69b7-e054-00144ff8d46c	2025-12-07	Warnings	Exact identifier application number: M001
Orange Antacid Soft Chew	CALCIUM CARBONATE	CVS Pharmacy	4a67f0d0-788b-433b-e054-00144ff88e88	2025-12-07	Warnings	Exact identifier application number: M001
Cherry Antacid Soft Chews	CALCIUM CARBONATE	CVS Pharmacy	61e4e83c-ee98-579d-e053-2991aa0ab099	2025-12-07	Warnings	Exact identifier application number: M001
CVS Mixed Berry Antacid HBG 54ct	CALCIUM CARBONATE	CVS Pharmacy	e9204edb-e4d9-3975-e053-2995a90ac6a9	2025-12-07	Warnings	Exact identifier application number: M001
CVS Mixed Berry Antacid HBG 28ct	CALCIUM CARBONATE	CVS Pharmacy	e9481d36-3b28-5caf-e053-2a95a90a3121	2025-12-07	Warnings	Exact identifier application number: M001
CVS Wild Berry Antacid Chews	CALCIUM CARBONATE	CVS Pharmacy	f6f45d9c-f9fc-225b-e053-6394a90a30e1	2025-12-07	Warnings	Exact identifier application number: M001
CVS Wild Berry Antacid Chews	CALCIUM CARBONATE	CVS Pharmacy	f6f5dc9a-b573-70c1-e053-6394a90acdb0	2025-12-07	Warnings	Exact identifier application number: M001
Basic Care Antacid Fruit Chews	CALCIUM CARBONATE	Amazon.com	c8d2b8aa-fce4-f973-e053-2995a90a6edd	2025-12-05	Warnings	Exact identifier application number: M001
Basic Care Berry Antacid HBG	CALCIUM CARBONATE	Amazon.com	c8d4050e-75fd-2445-e053-2995a90a7b0d	2025-12-05	Warnings	Exact identifier application number: M001
QUALITY CHOICE Regular Strength	ANTACID TABLETS (CALCIUM CARBONATE)	QUALITY CHOICE (Chain drug Marketing Assoiciation)	fce6c50d-908f-44a6-ba63-ece813f3711b	2025-12-04	Warnings	Exact identifier application number: M001
QUALITY CHOICE Regular Strength	ANTACID TABLETS (CALCIUM CARBONATE)	QUALITY CHOICE (Chain drug Marketing Assoiciation)	667ffb59-9bff-45a7-89f0-ccfa0d841909	2025-12-04	Warnings	Exact identifier application number: M001
QUALITY CHOICE	CALCIUM CARBONATE	QUALITY CHOICE (Chain drug Marketing Assoiciation)	9ff282fd-7623-4c9e-8faa-c51e33a7616e	2025-12-04	Warnings	Exact identifier application number: M001
QUALITY CHOICE Extra Strength	ANTACID TABLETS (CALCIUM CARBONATE)	QUALITY CHOICE (Chain drug Marketing Assoiciation)	7c948dc6-e569-46d2-8edd-59da48857e0e	2025-12-04	Warnings	Exact identifier application number: M001
QUALITY CHOICE Ultra Strength	ANTACID TABLETS (CALCIUM CARBONATE)	QUALITY CHOICE (Chain drug Marketing Assoiciation)	b074a885-5d10-46e4-8de9-dd9460968dad	2025-12-04	Warnings	Exact identifier application number: M001
Quality Choice Extra Strength	ANTACID TABLETS (CALCIUM CARBONATE)	QUALITY CHOICE (Chain drug Marketing Assoiciation)	2bb8ccb6-6275-4ace-8096-ee545501df39	2025-12-04	Warnings	Exact identifier application number: M001
Quality Choice Ultra Strength	ANTACID TABLET (CALCIUM CARBONATE)	QUALITY CHOICE (Chain drug Marketing Assoiciation)	cdac56f1-e579-4943-a24a-6564c30086d2	2025-12-04	Warnings	Exact identifier application number: M001
QUALITY CHOICE Original Flavor	ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE	CHAIN DRUG MARKETING ASSOCIATION INC.	a699b830-6400-4af9-9810-5eda79157333	2025-12-04	Warnings	Exact identifier application number: M001
Alka-Seltzer Heartburn Relief Peppermint	CALCIUM CARBONATE	Bayer HealthCare LLC.	9b8e802f-91b6-4559-e053-2a95a90aff67	2025-12-04	Warnings	Exact identifier application number: M001
Alka-Seltzer Cool Action Heartburn Relief Mint	CALCIUM CARBONATE	Bayer HealthCare LLC.	9b8da147-8d0c-e6b0-e053-2a95a90a35e6	2025-12-04	Warnings	Exact identifier application number: M001
Alka-Seltzer Kids Tummy ReliefChews	CALCIUM CARBONATE AND DIMETHICONE	Bayer HealthCare LLC.	ba48966e-3762-5fdf-e053-2995a90aeb3d	2025-12-04	Warnings	Exact identifier application number: M001

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5QB0T2IUN0	ALUMINUM HYDROXIDE	21645-51-2	ALUMINUM HYDROXIDE
NBZ3QY004S	MAGNESIUM HYDROXIDE	1309-42-8	MAGNESIUM HYDROXIDE
92RU3N3Y1O	DIMETHICONE	9006-65-9	DIMETHICONE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
307746	aluminum hydroxide 200 MG / magnesium hydroxide 200 MG / simethicone 20 MG in 5 mL Oral Suspension	PSN	043207dd-5e1c-4c78-b75a-7d341d71b117	6
307746	aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML / simethicone 4 MG/ML Oral Suspension	SCD	043207dd-5e1c-4c78-b75a-7d341d71b117	6
307746	aluminum hydroxide 1200 MG / milk of magnesia 1200 MG / dimethicone 120 MG per 30 ML Oral Suspension	SY	043207dd-5e1c-4c78-b75a-7d341d71b117	6
307746	aluminum hydroxide 200 MG / milk of magnesia 200 MG / dimethicone 20 MG per 5 ML Oral Suspension	SY	043207dd-5e1c-4c78-b75a-7d341d71b117	6
307746	aluminum hydroxide 400 MG / milk of magnesia 400 MG / dimethicone 40 MG per 10 ML Oral Suspension	SY	043207dd-5e1c-4c78-b75a-7d341d71b117	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
17856-0630-1	17856063001	50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0630-1) / 30 mL in 1 CUP, UNIT-DOSE	2024-05-06	0000-00-00	No	No	Current