NDC 76524-222 Nerve Pain Formula

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76524-222
Proprietary Name:
Nerve Pain Formula
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Protege' Media Llc
Labeler Code:
76524
Start Marketing Date: [9]
10-29-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76524-222-02

Package Description: 56 mL in 1 BOTTLE

Product Details

What is NDC 76524-222?

The NDC code 76524-222 is assigned by the FDA to the product Nerve Pain Formula which is product labeled by Protege' Media Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76524-222-02 56 ml in 1 bottle . 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 Nerve Pain Formula?

Liberally apply lotion to affected area and rub into joints.Use 3-4 times per day for the first week. Use as needed thereafter to relieve discomfort.Use no more than 4 times per day.Allow several days for product to take maximum effect.Use within 60 days from opening. Store at 50° to 75°F (10°C to 24°C)

Which are Nerve Pain Formula UNII Codes?

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

  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
  • CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D)
  • CANNABIS SATIVA SUBSP. SATIVA FLOWERING TOP (UNII: 8X454SZ22D) (Active Moiety)
  • AGKISTRODON PISCIVORUS VENOM (UNII: X9V1Q8U150)
  • AGKISTRODON PISCIVORUS VENOM (UNII: X9V1Q8U150) (Active Moiety)

Which are Nerve Pain Formula 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".