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  4. NDC Product Code: 21695-903 Magnesium Hydroxide

NDC 21695-903 Magnesium Hydroxide

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 21695-903?
  4. Magnesium Hydroxide Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
21695-903
Proprietary Name:
Magnesium Hydroxide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp
Labeler Code:
21695
Product Label ID:
c29995d6-e8f2-4e7b-aa03-6ce5aa0e7710
Start Marketing Date: [9]
03-22-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 21695-903?

The NDC code 21695-903 is assigned by the FDA to the product Magnesium Hydroxide which is product labeled by Rebel Distributors Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 21695-903-16 473 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Magnesium Hydroxide?

Laxative: ° shake well before using ° drink a full glass (8 ounces) of liquid with each dose ° may be taken as a single or divided doseAntacid: ° do not take more than 12 teaspoons in 24 hours ° do not use maximum dosage for more than 2 weeksLaxative:adults and children 12 years and older: 2 to 4 tablespoons children 6 to under 12 years: 1 to 2 tablespoonschildren 2 to under 6 years: 1 to 3 teaspoonschildren under 2 years: ask a doctorAntacid:adults and children 12 years and older: 1 to 3 teaspoons with water, up to 4 times dailychildren under 12 years: ask a doctor

Which are Magnesium Hydroxide UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Magnesium Hydroxide Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Magnesium Hydroxide?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 253017 - magnesium hydroxide 1200 MG in 15 mL Oral Suspension
  • RxCUI: 253017 - magnesium hydroxide 80 MG/ML Oral Suspension
  • RxCUI: 253017 - magnesium hydroxide 1200 MG per 15 ML Oral Suspension
  • RxCUI: 253017 - milk of magnesia 2400 MG per 30 ML Oral Suspension
  • RxCUI: 253017 - milk of magnesia 400 MG per 5 ML Oral Suspension

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".