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  5. NDC Package Code: 61821-001-01 Die Da Wan Hua Pain Relieving

NDC Package 61821-001-01 Die Da Wan Hua Pain Relieving

Turpentine Oil 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:
61821-001-01
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 50 mL in 1 BOTTLE, PLASTIC
Product Code:
61821-001
Proprietary Name:
Die Da Wan Hua Pain Relieving
Non-Proprietary Name:
Turpentine
Substance Name:
Turpentine
11-Digit NDC Billing Format:
61821000101
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Baiyunshan Jingxiutang Pharmaceutical Co., Ltd
Dosage Form:
Oil - An unctuous, combustible substance which is liquid, or easily liquefiable, on warming, and is soluble in ether but insoluble in water. Such substances, depending on their origin, are classified as animal, mineral, or vegetable oils.
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):
  • TURPENTINE 6 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    05-08-2003
    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 61821-001-01?

    The NDC Packaged Code 61821-001-01 is assigned to a package of 1 bottle, plastic in 1 box / 50 ml in 1 bottle, plastic of Die Da Wan Hua Pain Relieving, a human over the counter drug labeled by Guangzhou Baiyunshan Jingxiutang Pharmaceutical Co., Ltd. The product's dosage form is oil and is administered via topical form.

    Is NDC 61821-001 included in the NDC Directory?

    Yes, Die Da Wan Hua Pain Relieving with product code 61821-001 is active and included in the NDC Directory. The product was first marketed by Guangzhou Baiyunshan Jingxiutang Pharmaceutical Co., Ltd on May 08, 2003 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 61821-001-01?

    The 11-digit format is 61821000101. 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
    5-3-261821-001-015-4-261821-0001-01