MINTOX MAXIMUM STRENGTH

Product NDC: 17856-5725
11-digit product format: 178565725
Labeler code: 17856
Product ID: 17856-5725_3b3f429e-d2e4-441c-e063-6294a90aaf4d
Type: HUMAN OTC DRUG
Nonproprietary name: aluminum hydroxide, magnesium hydroxide, dimethicone
Dosage form: SUSPENSION
Route: ORAL
Labeler: ATLANTIC BIOLOGICALS CORP.
Application: M
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-02-01
Substance: ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE
Active strength: 400; 400; 40 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

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	17856-5725	17856-5725-1	D	Discontinued by firm		2026-10-12

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 · 14 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	17856-5725-1	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	17856-5725-1	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	17856-5725-1	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	17856-5725-3	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	17856-5725-1	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	17856-5725-3	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	17856-5725-1	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	17856-5725-3	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	17856-5725-1	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	17856-5725-3	I	Inactivated by FDA	`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: MINTOX MAXIMUM STRENGTH
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ALUMINUM HYDROXIDE	400 mg/5mL
MAGNESIUM HYDROXIDE	400 mg/5mL
DIMETHICONE	40 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 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
237870	Internal RxNorm lookup
708127	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
ac6a47e7-972f-4b82-96da-89926d345e9f	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
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
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
17856-5725-1	2024-07-30	Mintox Max
17856-5725-3	2024-07-30	Mintox Max
17856-5725-1	2023-01-30	Mintox Max
17856-5725-3	2023-01-30	Mintox Max

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
17856-5725-1	MINTOX MAXIMUM STRENGTH	15 mL in 1 CUP	SUSPENSION	15		9
17856-5725-3	MINTOX MAXIMUM STRENGTH	30 mL in 1 CUP	SUSPENSION	30		9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
17856-5725-3	ML - Milliliter	17856-5725	450f9c1d-edc9-4c3f-91ab-6b5580bf91bc	1	2014-09-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALUMINUM HYDROXIDE	ACTIVE INGREDIENT	5QB0T2IUN0	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
DIMETHICONE	ACTIVE INGREDIENT	92RU3N3Y1O	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
MAGNESIUM HYDROXIDE	ACTIVE INGREDIENT	NBZ3QY004S	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
ALUMINUM HYDROXIDE	ACTIVE MOIETY	5QB0T2IUN0	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
DIMETHICONE	ACTIVE MOIETY	92RU3N3Y1O	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
HYDROXIDE ION	ACTIVE MOIETY	9159UV381P	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
BUTYLPARABEN	INACTIVE INGREDIENT	3QPI1U3FV8	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
SACCHARIN SODIUM	INACTIVE INGREDIENT	SB8ZUX40TY	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
SORBITOL	INACTIVE INGREDIENT	506T60A25R	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORPS]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17856-5725	MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [ATLANTIC BIOLOGICALS CORP.]	8	Current NDC, Legacy NDC, 2 package rows	20250524_ac6a47e7-972f-4b82-96da-89926d345e9f.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 4 of 6 · 111 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
First Street Antibacterial Liquid Hand	BENZALKONIUM CHLORIDE	Amerifoods Trading Company	e9d5fefa-970b-42ba-8139-18e564415344	2025-11-06	Warnings	Exact identifier application number: M
Cetirza	CETIRIZINE HCL	HART Health	44b22f6f-5731-4dfe-af33-4e4e54fc3af5	2025-10-06	Warnings	Exact identifier application number: M
Dolce and Gabbana Blueberry Nutri Tint SPF 20 6W Light	ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	d2930d0e-c622-4843-87f2-fa1a92837ff2	2025-09-05	Warnings	Exact identifier application number: M
Alcohol	ISOPROPYL ALCOHOL	NorMed	959815e5-a73b-4905-9d7d-904b33498386	2025-08-15	Warnings	Exact identifier application number: M
TRIBIOTIC	BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE	HART Health	c1903b9f-390a-4756-800c-fd93be4182e3	2025-08-13	Warnings, Adverse reactions	Exact identifier application number: M
THERASTAT	CHERRY COUGH DROPS	HART Health	96bae19a-3337-4199-9b8c-cdf9b368178b	2025-08-04	Warnings	Exact identifier application number: M
Docu Liquid	DOCUSATE SODIUM	ATLANTIC BIOLOGICALS CORP.	f4ed0721-3be9-4108-a6c9-dbbe115249e9	2025-07-31	Warnings	Exact identifier application number: M
MINTOX MAXIMUM STRENGTH	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE	ATLANTIC BIOLOGICALS CORP.	ac6a47e7-972f-4b82-96da-89926d345e9f	2025-07-31	Warnings	Exact identifier application number: M ndc (product): 17856-5725
SENNA	SENNA	ATLANTIC BIOLOGICALS CORP.	8b7cc0d5-029b-43f7-a050-8771e7db4551	2025-07-31	Warnings	Exact identifier application number: M
Stimulant Laxative Plus Stool Softener	DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG	ATLANTIC BIOLOGICALS CORP.	4c02fcec-6bb7-4497-96c5-0d809209dd17	2025-06-27	Warnings	Exact identifier application number: M
Orythia Pain Relieving Lidocaine	LIDOCAINE	Planet (Anhui) Pharmaceutical Co., Ltd.	d658d495-dd2c-40b7-9446-6f10040ed55e	2025-06-27	Warnings	Exact identifier application number: M
Bonica EaseX Pain Relieving	CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE	Planet (Anhui) Pharmaceutical Co., Ltd.	34f1196a-fda1-4bef-be71-e5a09ee97bc1	2025-06-27	Warnings	Exact identifier application number: M
Regular Strength Enteric coated aspirin	ASPIRIN	ATLANTIC BIOLOGICALS CORP.	e1c8d0ed-da1d-4b1a-9a85-7b8532775f87	2025-06-24	Warnings	Exact identifier application number: M
Aspirin Low Dose Chewable Orange	ASPIRIN	ATLANTIC BIOLOGICALS CORP.	a0d8ee59-1ce0-4ddd-a90c-54adb512540c	2025-06-24	Warnings	Exact identifier application number: M
Hydrogen Peroxide	HYDROGEN PEROXIDE	HART Health	f50af223-ba83-458a-a557-1ba5dc221a9c	2025-06-10	Warnings	Exact identifier application number: M
Pharbetol Regular strength	ACETAMINOPHEN	ATLANTIC BIOLOGICALS CORP.	05a91d24-b498-4ba2-a275-68b871cf62d2	2025-06-05	Warnings	Exact identifier application number: M
TEENY TUMMY Gas Relief Drops	SIMETHICONE	ATLANTIC BIOLOGICALS CORP	376660a2-becb-48cf-a9f5-6a76a8b8ca70	2025-05-30	Warnings	Exact identifier application number: M
Mineral Oil	MINERAL OIL	ATLANTIC BIOLOGICALS CORP.	960502ae-2468-406e-8799-cacb01f2727e	2025-05-23	Warnings	Exact identifier application number: M
Stomach Relief Regular Strength	BISMUTH SUBSALICYLATE	ATLANTIC BIOLOGICALS CORP.	5c02d0ba-91e4-4bd2-ac66-6905323653b2	2025-05-12	Warnings	Exact identifier application number: M
MAX Tussin Cough and Chest Congestion DM Sugar Free	DEXTROMETHORPHAN HBR, GUAIFENESIN	ATLANTIC BIOLOGICALS CORP.	8f496c61-41a6-41ba-80f5-7a5309c4d18b	2025-05-12	Warnings	Exact identifier application number: M

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
237870	aluminum hydroxide 400 MG / magnesium hydroxide 400 MG / simethicone 40 MG in 5 mL Oral Suspension	PSN	ac6a47e7-972f-4b82-96da-89926d345e9f	9
708127	Mintox Maximum Strength 400 MG / 400 MG / 40 MG in 5 mL Oral Suspension	PSN	ac6a47e7-972f-4b82-96da-89926d345e9f	9
708127	aluminum hydroxide 80 MG/ML / magnesium hydroxide 80 MG/ML / simethicone 8 MG/ML Oral Suspension [Mintox Plus]	SBD	ac6a47e7-972f-4b82-96da-89926d345e9f	9
237870	aluminum hydroxide 80 MG/ML / magnesium hydroxide 80 MG/ML / simethicone 8 MG/ML Oral Suspension	SCD	ac6a47e7-972f-4b82-96da-89926d345e9f	9
237870	aluminum hydroxide 2400 MG / magnesium hydroxide 2400 MG / dimethicone 240 MG per 30 ML Oral Suspension	SY	ac6a47e7-972f-4b82-96da-89926d345e9f	9
237870	aluminum hydroxide 400 MG / magnesium hydroxide 400 MG / simethicone 40 MG per 5 ML Oral Suspension	SY	ac6a47e7-972f-4b82-96da-89926d345e9f	9
237870	aluminum hydroxide 800 MG / magnesium hydroxide 800 MG / dimethicone 80 MG per 10 ML Oral Suspension	SY	ac6a47e7-972f-4b82-96da-89926d345e9f	9
708127	Mintox (aluminum hydroxide 400 MG / milk of magnesia 400 MG / simethicone 40 MG) per 5 ML Oral Suspension	SY	ac6a47e7-972f-4b82-96da-89926d345e9f	9
708127	Mintox Maximum Strength (aluminum hydroxide 80 MG/ML / magnesium hydroxide 80 MG/ML / simethicone 8 MG/ML) Oral Suspension	SY	ac6a47e7-972f-4b82-96da-89926d345e9f	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
17856-5725-1	17856572501	15 mL in 1 CUP (17856-5725-1)	15 ml	2021-01-28	0000-00-00	No	No	Current
17856-5725-3	17856572503	30 mL in 1 CUP (17856-5725-3)	30 ml	2021-01-28	0000-00-00	No	No	Current