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  4. NDC Product Code: 70072-003 Elf Perm

NDC 70072-003 Elf Perm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70072-003?
  4. Elf Perm 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:
70072-003
Proprietary Name:
Elf Perm
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Giod Co.
Labeler Code:
70072
Product Label ID:
6645ae29-0c6d-4632-b972-482df7df098c
Start Marketing Date: [9]
09-05-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70072-003?

The NDC code 70072-003 is assigned by the FDA to the product Elf Perm which is product labeled by Giod Co.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70072-003-02 1 container in 1 carton / 479.39 g in 1 container (70072-003-01). 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 Elf Perm?

Shampoo and remove excessive moisture from hair with a towelApply the first solution and roll hair in curlersAllow 10 minutes of heat treatment (Adjust ±5-10 minutes depends on the time needed)Apply second solution and rinse

Which are Elf Perm UNII Codes?

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

Which are Elf Perm 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".