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  4. NDC Product Code: 71486-3050 Glint

NDC 71486-3050 Glint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71486-3050?
  4. Glint 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:
71486-3050
Proprietary Name:
Glint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Glint Cosmetics Private Limited
Labeler Code:
71486
Product Label ID:
64e395b7-4ea3-5964-e053-2a91aa0a750d
Start Marketing Date: [9]
05-23-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 71486-3050?

The NDC code 71486-3050 is assigned by the FDA to the product Glint which is product labeled by Glint Cosmetics Private Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71486-3050-2 .9 g in 1 packet , 71486-3050-3 28.3 g in 1 tube . 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 Glint?

■ adults and children over 2 years of age■ apply evenly to affected area no more than 3 to 4 times daily■ children under 2 years of age■ do not use, consult a doctor ■ adults and children over 2 years of age■ apply evenly to affected area no more than 3 to 4 times daily■ children under 2 years of age■ do not use, consult a doctor■ Adults■ when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly■ gently dry, patting or blotting with bathroom tissue or soft cloth before applying■ apply externally to the area up to 6 times a daily or after a bowel movement■ after application discard pad■ do not flush in toilet

Which are Glint UNII Codes?

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

Which are Glint 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 Glint?

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:

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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".