NDC 62011-0123 Milk Of Magnesia Mint

Magnesium Hydroxide

NDC Product Code 62011-0123

NDC CODE: 62011-0123

Proprietary Name: Milk Of Magnesia Mint What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Magnesium Hydroxide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used for a short time to treat occasional constipation. It is a laxative (osmotic-type) that is thought to work by drawing water into the intestines, an effect that helps to cause movement of the intestines. This medication is also used to treat symptoms caused by too much stomach acid such as heartburn, upset stomach, or indigestion. It is an antacid that works by lowering the amount of acid in the stomach.

Product Characteristics

Flavor(s):
MINT (C73404 - MINT)

NDC Code Structure

  • 62011 - Strategic Sourcing Services Llc

NDC 62011-0123-1

Package Description: 355 mL in 1 BOTTLE

Price per Unit: $0.00657 per ML

NDC Product Information

Milk Of Magnesia Mint with NDC 62011-0123 is a a human over the counter drug product labeled by Strategic Sourcing Services Llc. The generic name of Milk Of Magnesia Mint is magnesium hydroxide. The product's dosage form is liquid and is administered via oral form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 253017.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Milk Of Magnesia Mint Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)
  • SACCHARIN (UNII: FST467XS7D)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Strategic Sourcing Services Llc
Labeler Code: 62011
FDA Application Number: part334 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 04-01-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Information for Patients

Magnesium Hydroxide

Magnesium Hydroxide is pronounced as (mag nee' zee um) (hye drox' ide)

Why is magnesium hydroxide medication prescribed?
Magnesium hydroxide is used on a short-term basis to treat constipation.This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more inf...
[Read More]

* Please review the disclaimer below.

Milk Of Magnesia Mint Product Label Images

Milk Of Magnesia Mint Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient (1 Tablespoon)

Magnesium hydroxide 1200 mg

Purpose

Saline laxative

Uses

  • Relieves occasional constipation (irregularity)generally
  • Produces bowel movement in 1/2 to 6 hours

Warnings

  • Ask a doctor before use if you havekidney diseasea magnesium-restricted dietstomach pain, nausea, or vomitinga sudden change in bowel habits that lasts more than 14 daysAsk a doctor or pharmacist before use if you are presently taking a prescription drug.
  • This product may interact with certain prescription drugs.Stop use and ask a doctor ifyou have rectal bleeding or failure to have a bowel movement after using this product. These could be signs of a serious condition.you need to use a laxative for more than 1 weekIf pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

  • Shake well before usedo not exceed the maximum recommended daily dose in a 24 hour perioddose may be taken once a day preferably at bedtime, in divided doses, or as directed by a doctordrink a full glass (8 oz) of liquid with each doseadults and children 12 years and over2 to 4 tablespoonfuls (TBSP)children 6 to 11 years1 to 2 tablespoonfuls (TBSP)children under 6 yearsask a doctor

Other Information




each tablespoon contains: magnesium 500 mg


• do not freeze • store at room temperature tightly closed

Inactive Ingredients

Flavor, purified water, saccharin sodium, sodium hypochlorite

* Please review the disclaimer below.