NDC Package 58368-002-02 Neorelief For Muscle Crampling And Restlessness

Topical Gel For Muscle Cramping And Restlessness Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
58368-002-02
Package Description:
56.7 g in 1 BOTTLE, PUMP
Product Code:
Proprietary Name:
Neorelief For Muscle Crampling And Restlessness
Non-Proprietary Name:
Topical Gel For Muscle Cramping And Restlessness
Substance Name:
Arnica Montana; Artemisia Cina Pre-flowering Top; Atropa Belladonna Root; Black Cohosh; Causticum; Frangula Californica Bark; Hypericum Perforatum; Jatropha Curcas Seed; Lycopodium Clavatum Spore; Potassium Bromide; Potassium Carbonate; Pseudognaphalium Obtusifolium; Ruta Graveolens Flowering Top; Scutellaria Lateriflora; Strychnos Ignatii Seed; Taraxacum Officinale; Valerian; Veratrum Album Root
Usage Information:
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.
11-Digit NDC Billing Format:
58368000202
Product Type:
Human Otc Drug
Labeler Name:
Biolyte Laboratories, Llc
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
02-01-2017
Listing Expiration Date:
12-31-2025
Exclude Flag:
N

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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Frequently Asked Questions

What is NDC 58368-002-02?

The NDC Packaged Code 58368-002-02 is assigned to a package of 56.7 g in 1 bottle, pump of Neorelief For Muscle Crampling And Restlessness, a human over the counter drug labeled by Biolyte Laboratories, Llc. The product's dosage form is gel and is administered via topical form.

Is NDC 58368-002 included in the NDC Directory?

Yes, Neorelief For Muscle Crampling And Restlessness with product code 58368-002 is active and included in the NDC Directory. The product was first marketed by Biolyte Laboratories, Llc on February 01, 2017 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 58368-002-02?

The 11-digit format is 58368000202. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-258368-002-025-4-258368-0002-02