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  4. NDC Product Code: 60512-8037 Diamite 12

NDC 60512-8037 Diamite 12

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 60512-8037?
  5. Diamite 12 Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
60512-8037
Proprietary Name:
Diamite 12
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Homeolab Usa Inc
Labeler Code:
60512
Product Label ID:
d4aeca9c-e01f-4c4e-89e0-5e0f6639c799
Start Marketing Date: [9]
06-12-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
8 MM
Imprint(s):
NONE
Score:
1

Code Structure Chart

Product Details

What is NDC 60512-8037?

The NDC code 60512-8037 is assigned by the FDA to the product Diamite 12 which is product labeled by Homeolab Usa Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60512-8037-7 5000 tablet, chewable in 1 container . 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 Diamite 12?

Children from 2 to 5 years: Crush 2 tablets and dissolve in water 3 times daily, or as directed by a healthcare professional.Adults and children over 5 years: Chew 2 tablets 3 times daily, or as directed by a healthcare professional.• Do not use more than directed.• Do not take with food.

Which are Diamite 12 UNII Codes?

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

Which are Diamite 12 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:

* Please review the disclaimer below.

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".