NDC 58368-002 Neorelief For Muscle Crampling And Restlessness

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:
58368-002
Proprietary Name:
Neorelief For Muscle Crampling And Restlessness
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Biolyte Laboratories, Llc
Labeler Code:
58368
Start Marketing Date: [9]
02-01-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 58368-002-02

Package Description: 56.7 g in 1 BOTTLE, PUMP

Product Details

What is NDC 58368-002?

The NDC code 58368-002 is assigned by the FDA to the product Neorelief For Muscle Crampling And Restlessness which is product labeled by Biolyte Laboratories, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58368-002-02 56.7 g 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 Neorelief For Muscle Crampling And Restlessness?

Adults and children 2 years of age and older, apply a thin layer of gel on clean skin to cover the affected area. For best results, allow gel to be absorbed into the skin; do not rub in. Apply at the onset of symptoms, not more than 6 times daily or every 15 minutes for the first hour. Do not use with other topical remedies or lotions.

Which are Neorelief For Muscle Crampling And Restlessness UNII Codes?

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

Which are Neorelief For Muscle Crampling And Restlessness 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".