Acid Reflux Relief Pellet
NDC Package 61727-331-21

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Acid Reflux Relief (capsicum, sodium phosphate, dibasic, heptahydrate, strychnos nux-vomica seed, robinia pseudoacacia bark, sulfur, sepia officinalis juice) pellets is turn tube upside down, twist cap to break seal & release pellets. This formulation utilizes a pellet delivery system. Marketed by Homeocare Laboratories, this product is identified by NDC 61727-331.

Identification & Billing

NDC Package Code
61727-331-21
Package Description
4 g in 1 TUBE
Product Code
61727-331
11-Digit Billing Format
61727033121

Clinical Specifications

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
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
Sublingual - Administration beneath the tongue.
Active Ingredient(s)
Pharmacologic Class
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.

Regulatory & Marketing

Labeler Name
Homeocare Laboratories
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-08-2012
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 61727-331-21 identifies a specific commercial package of 4 g in 1 tube of Acid Reflux Relief, a human over the counter drug labeled by Homeocare Laboratories. This pellet is formulated for sublingual use and contains capsicum; robinia pseudoacacia bark; sepia officinalis juice; sodium phosphate, dibasic, heptahydrate; strychnos nux-vomica seed; sulfur as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Homeocare Laboratories on June 08, 2012. The current certification is valid through December 31, 2026.

How is this Homeocare Laboratories product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61727033121. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
61727-331-21
11-Digit CMS (5-4-2)
61727-0331-21

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.