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  4. NDC Product Code: 76348-576 Ak47 Menthol Cooling Cream Packet

NDC 76348-576 Ak47 Menthol Cooling Cream Packet

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76348-576?
  4. Ak47 Menthol Cooling Cream Packet 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:
76348-576
Proprietary Name:
Ak47 Menthol Cooling Cream Packet
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Renu Laboratories, Inc.
Labeler Code:
76348
Product Label ID:
adb83c12-6e29-8c70-e053-2a95a90a2761
Start Marketing Date: [9]
08-13-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 76348-576?

The NDC code 76348-576 is assigned by the FDA to the product Ak47 Menthol Cooling Cream Packet which is product labeled by Renu Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76348-576-10 10 packet in 1 box / 4 g in 1 packet (76348-576-04). 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 Ak47 Menthol Cooling Cream Packet?

Usesfor temporary relief of minor aches and pains of muscles and joints associated withbruisessprainsarthritisstrains

Which are Ak47 Menthol Cooling Cream Packet UNII Codes?

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

Which are Ak47 Menthol Cooling Cream Packet 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".