NDC Package 49873-068-02 Satohap

Methyl Salicylate,Dl-camphor,L-menthol Spray 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:
49873-068-02
Package Description:
70 mL in 1 CANISTER
Product Code:
Proprietary Name:
Satohap
Non-Proprietary Name:
Methyl Salicylate, Dl-camphor, L-menthol
Substance Name:
Camphor (synthetic); Levomenthol; Methyl Salicylate
Usage Information:
Uses   temporary relieves minor aches and pains of muscles and joints due to ■ backache   ■ arthritis   ■ strains   ■ bruises   ■sprains
11-Digit NDC Billing Format:
49873006802
NDC to RxNorm Crosswalk:
  • RxCUI: 1249174 - camphor 5 % / menthol 4 % / methyl salicylate 10 % Topical Spray
  • RxCUI: 1249174 - camphor 50 MG/ML / menthol 40 MG/ML / methyl salicylate 100 MG/ML Topical Spray
  • RxCUI: 1249176 - SATOHAP 5 % / 4 % / 10 % Topical Spray
  • RxCUI: 1249176 - camphor 50 MG/ML / menthol 40 MG/ML / methyl salicylate 100 MG/ML Topical Spray [Satohap]
  • RxCUI: 1249176 - Satohap (camphor 5 % / menthol 4 % / methyl salicylate 10 % ) Topical Spray
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Sato Pharmaceutical Co., Ltd.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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:
    11-03-2006
    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.

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    Frequently Asked Questions

    What is NDC 49873-068-02?

    The NDC Packaged Code 49873-068-02 is assigned to a package of 70 ml in 1 canister of Satohap, a human over the counter drug labeled by Sato Pharmaceutical Co., Ltd.. The product's dosage form is spray and is administered via topical form.

    Is NDC 49873-068 included in the NDC Directory?

    Yes, Satohap with product code 49873-068 is active and included in the NDC Directory. The product was first marketed by Sato Pharmaceutical Co., Ltd. on November 03, 2006 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 49873-068-02?

    The 11-digit format is 49873006802. 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
    5-3-249873-068-025-4-249873-0068-02