NDC 77496-101 Prologel Pain Relief

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:
77496-101
Proprietary Name:
Prologel Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nova Neura, Llc
Labeler Code:
77496
Start Marketing Date: [9]
12-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 77496-101-11

Package Description: 148 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 77496-101?

The NDC code 77496-101 is assigned by the FDA to the product Prologel Pain Relief which is product labeled by Nova Neura, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 77496-101-11 148 ml in 1 bottle, pump . 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 Prologel Pain Relief?

Shake well before each use. Keep cap on between uses.Adults and children 12 years of age or older:Apply generous amount to clean, unbroken skin.Allow lotion to rest on skin for approximately one minuteRub lotion into the target area.Reapply up to four times per day.Wash hands thoroughly after each application.

Which are Prologel Pain Relief UNII Codes?

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

Which are Prologel Pain 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".