NDC Package 27854-499-01 Flanax

Methyl Salicylate,Menthol,Capsaicin Liniment 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:
27854-499-01
Package Description:
1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
Product Code:
Proprietary Name:
Flanax
Non-Proprietary Name:
Methyl Salicylate, Menthol, Capsaicin
Substance Name:
Capsaicin; Menthol, Unspecified Form; Methyl Salicylate
Usage Information:
Adults and children 12 years of age and older: Apply to affected area not more than 3-4 times daily. A temporary burning may be felt when applied, but usually disappears with continued use. Wash hands thoroughly after use to avoid spreading liniment to the eyes or other sensitive areas of the body. If applying liniment to the hands wait 30 minutes before washing hands. Initial pain relief is usually noted within 1-2 weeks. If condition does not improve in 4 weeks discontinue use of this product. Children under 12 years of age: consult doctor before use. 
11-Digit NDC Billing Format:
27854049901
Product Type:
Human Otc Drug
Labeler Name:
Belmora Llc
Dosage Form:
Liniment - A solution or mixture of various substances in oil, alcoholic solutions of soap, or emulsions intended for external application.
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
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-01-2024
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 27854-499-01?

The NDC Packaged Code 27854-499-01 is assigned to a package of 1 tube in 1 carton / 28.35 g in 1 tube of Flanax, a human over the counter drug labeled by Belmora Llc. The product's dosage form is liniment and is administered via topical form.

Is NDC 27854-499 included in the NDC Directory?

Yes, Flanax with product code 27854-499 is active and included in the NDC Directory. The product was first marketed by Belmora Llc on August 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 27854-499-01?

The 11-digit format is 27854049901. 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
5-3-227854-499-015-4-227854-0499-01