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  4. NDC Product Code: 12753-930 999 Itch Relief

NDC 12753-930 999 Itch Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 12753-930?
  4. 999 Itch Relief Uses
  5. Active Ingredients UNII Codes
  6. 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:
12753-930
Proprietary Name:
999 Itch Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
China Resources Sanjiu Medical & Pharmaceutical Co Ltd
Labeler Code:
12753
Product Label ID:
d2390d79-4a64-4773-926b-3ebcdc0727f9
Start Marketing Date: [9]
07-03-2003
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 12753-930?

The NDC code 12753-930 is assigned by the FDA to the product 999 Itch Relief which is product labeled by China Resources Sanjiu Medical & Pharmaceutical Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 12753-930-19 20000 mg in 1 carton . 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 999 Itch Relief?

Pregnant and children under 2 years of age. Do not use, consult a doctor. Adult and children 2 years of age and older. Apply liberally to affected area not more than 5 times daily and 5-8 times per day for some severe cases or follow doctor's instruction.

Which are 999 Itch Relief UNII Codes?

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

Which are 999 Itch Relief 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:

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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".