MILK OF MAGNESIA MINT

Product NDC: 62011-0123
Requested package NDC: 62011-0123-1
11-digit product format: 620110123
Labeler code: 62011
Product ID: 62011-0123_9a9d92ef-79a6-629a-e053-2995a90afd58
Type: HUMAN OTC DRUG
Nonproprietary name: magnesium hydroxide
Dosage form: LIQUID
Route: ORAL
Labeler: STRATEGIC SOURCING SERVICES LLC
Application: part334
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2012-04-01
Marketing end: 0000-00-00
Substance: MAGNESIUM HYDROXIDE
Active strength: 1200 mg/15mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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	62011-0123	62011-0123-1	D	Discontinued by firm		2026-10-05

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	62011-0123	62011-0123-1	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	62011-0123	62011-0123-1	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62011-0123-1	ML - Milliliter	62011-0123	e88ed56b-aa1d-4e69-a9c3-5fd1724ab442	1	2014-11-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
MAGNESIUM HYDROXIDE	ACTIVE INGREDIENT	NBZ3QY004S	MILK OF MAGNESIA MINT (MAGNESIUM HYDROXIDE) LIQUID [MCKESSON]	1
HYDROXIDE ION	ACTIVE MOIETY	9159UV381P	MILK OF MAGNESIA MINT (MAGNESIUM HYDROXIDE) LIQUID [MCKESSON]	1
SACCHARIN SODIUM DIHYDRATE	INACTIVE INGREDIENT	SB8ZUX40TY	MILK OF MAGNESIA MINT (MAGNESIUM HYDROXIDE) LIQUID [MCKESSON]	1
SODIUM HYPOCHLORITE	INACTIVE INGREDIENT	DY38VHM5OD	MILK OF MAGNESIA MINT (MAGNESIUM HYDROXIDE) LIQUID [MCKESSON]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	MILK OF MAGNESIA MINT (MAGNESIUM HYDROXIDE) LIQUID [MCKESSON]	1

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
NBZ3QY004S	MAGNESIUM HYDROXIDE	1309-42-8	MAGNESIUM HYDROXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
62011-0123-1	62011012301	355 mL in 1 BOTTLE (62011-0123-1)	355 ml	2017-09-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
health mart mom mint	STRATEGIC SOURCING SERVICES LLC \| GCP Laboratories	2023-11-07	HUMAN OTC DRUG LABEL	4