Arctic Blast Pain Releiving Liquid
NDC Package 71856-176-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Arctic Blast Pain Releiving (menthol, camphor (synthetic)) liquids is for the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains. This formulation utilizes a liquid delivery system. Marketed by Nutriomo Labs Pte, Ltd, this product is identified by NDC 71856-176 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
71856-176-01
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
71856-176
11-Digit Billing Format
71856017601
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Arctic Blast Pain Releiving
Non-Proprietary Name
Menthol, Camphor (synthetic)
Substance Name
Camphor (synthetic); Menthol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.

Regulatory & Marketing

Labeler Name
Nutriomo Labs Pte, Ltd
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-01-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 71856-176-01 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Arctic Blast Pain Releiving, a human over the counter drug labeled by Nutriomo Labs Pte, Ltd. This liquid is formulated for topical use and contains camphor (synthetic); menthol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Nutriomo Labs Pte, Ltd on May 01, 2018. The current certification is valid through December 31, 2026.

How is this Nutriomo Labs Pte, Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71856017601. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
71856-176-01
11-Digit CMS (5-4-2)
71856-0176-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.