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  5. NDC Package Code: 71856-176-01 Arctic Blast Pain Releiving

NDC Package 71856-176-01 Arctic Blast Pain Releiving

Menthol,Camphor (synthetic) Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
71856-176-01
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
71856-176
Proprietary Name:
Arctic Blast Pain Releiving
Non-Proprietary Name:
Menthol, Camphor (synthetic)
Substance Name:
Camphor (synthetic); Menthol
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.
11-Digit NDC Billing Format:
71856017601
NDC to RxNorm Crosswalk:
  • RxCUI: 1987413 - camphor 3 % / menthol 10 % Topical Solution
  • RxCUI: 1987413 - camphor 30 MG/ML / menthol 100 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Nutriomo Labs Pte, Ltd
    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(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.
    • Active Ingredient(s):
  • CAMPHOR (SYNTHETIC) 30 mg/mL
  • MENTHOL 100 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    05-01-2018
    Listing Expiration Date:
    12-31-2024
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71856-176-01?

    The NDC Packaged Code 71856-176-01 is assigned to a 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. The product's dosage form is liquid and is administered via topical form.

    Is NDC 71856-176 included in the NDC Directory?

    Yes, Arctic Blast Pain Releiving with product code 71856-176 is active and included in the NDC Directory. The product was first marketed by Nutriomo Labs Pte, Ltd on May 01, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71856-176-01?

    The 11-digit format is 71856017601. 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
    5-3-271856-176-015-4-271856-0176-01