NDC Package 61727-330-21 Hangover Relief

Asafetida, Capsicum, Potassium Dichromate, Cola Nut, Lachesis Muta Venom, Strychnos - 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:
61727-330-21
Package Description:
4 g in 1 TUBE
Product Code:
Proprietary Name:
Hangover Relief
Non-Proprietary Name:
Asafetida, Capsicum, Potassium Dichromate, Cola Nut, Lachesis Muta Venom, Strychnos Nux-vomica Seed, Ranunculus Bulbosus, Sulfuric Acid, Zinc.
Substance Name:
Asafetida; Capsicum; Cola Nut; Lachesis Muta Venom; Potassium Dichromate; Ranunculus Bulbosus; Strychnos Nux-vomica Seed; Sulfuric Acid; Zinc
Usage Information:
This product is used as For the temporary relief of headache, nausea and vomiting associated with alcohol consumption.. For the temporary relief of headache, nausea and vomiting associated with alcohol consumption.
11-Digit NDC Billing Format:
61727033021
Product Type:
Human Otc Drug
Labeler Name:
Homeocare Laboratories
Dosage Form:
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route(s):
  • Sublingual - Administration beneath the tongue.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    11-23-2011
    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 61727-330-21?

    The NDC Packaged Code 61727-330-21 is assigned to a package of 4 g in 1 tube of Hangover Relief, a human over the counter drug labeled by Homeocare Laboratories. The product's dosage form is pellet and is administered via sublingual form.

    Is NDC 61727-330 included in the NDC Directory?

    Yes, Hangover Relief with product code 61727-330 is active and included in the NDC Directory. The product was first marketed by Homeocare Laboratories on November 23, 2011 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 61727-330-21?

    The 11-digit format is 61727033021. 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
    5-3-261727-330-215-4-261727-0330-21