NDC Package 61727-331-21 Acid Reflux Relief

Capsicum,Sodium Phosphate,Dibasic,Heptahydrate,Strychnos Nux-vomica Seed,Robinia - 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:
61727-331-21
Package Description:
4 g in 1 TUBE
Product Code:
Proprietary Name:
Acid Reflux Relief
Non-Proprietary Name:
Capsicum, Sodium Phosphate, Dibasic, Heptahydrate, Strychnos Nux-vomica Seed, Robinia Pseudoacacia Bark, Sulfur, Sepia Officinalis Juice
Substance Name:
Capsicum; Robinia Pseudoacacia Bark; Sepia Officinalis Juice; Sodium Phosphate, Dibasic, Heptahydrate; Strychnos Nux-vomica Seed; Sulfur
Usage Information:
Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue before meals or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.
11-Digit NDC Billing Format:
61727033121
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:
    06-08-2012
    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 61727-331-21?

    The NDC Packaged Code 61727-331-21 is assigned to a package of 4 g in 1 tube of Acid Reflux 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 61727-331 included in the NDC Directory?

    Yes, Acid Reflux Relief with product code 61727-331 is active and included in the NDC Directory. The product was first marketed by Homeocare Laboratories on June 08, 2012 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 61727-331-21?

    The 11-digit format is 61727033121. 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
    5-3-261727-331-215-4-261727-0331-21