Biophresh Suppository
NDC Package 73716-001-10

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

Package Information

Biophresh (kreosotum 6c, nitricum acidum 6c, thuja occidentalis 6c, pulsatilla vulgaris 6c, sepia officinalis 6c) suppositories is uses for the temporary relief of symptoms of bacterial vaginosis due to bacterial imbalance in the vagina including vaginal odor, itching, irritaiton, or abnormal discharge. This formulation utilizes a suppository delivery system. Marketed by Good Clean Love, Inc., this product is identified by NDC 73716-001.

Identification & Billing

NDC Package Code
73716-001-10
Package Description
1 g in 1 BLISTER PACK
Product Code
73716-001
11-Digit Billing Format
73716000110

Clinical Specifications

Proprietary Name
Biophresh
Non-Proprietary Name
Kreosotum 6c, Nitricum Acidum 6c, Thuja Occidentalis 6c, Pulsatilla Vulgaris 6c, Sepia Officinalis 6c
Substance Name
Nitric Acid; Pulsatilla Vulgaris; Sepia Officinalis Whole; Thuja Occidentalis Leafy Twig; Wood Creosote
Dosage Form
Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
Administration Route
Vaginal - Administration into the vagina.
Active Ingredient(s)
Usage Information
Uses for the temporary relief of symptoms of bacterial vaginosis due to bacterial imbalance in the vagina including vaginal odor, itching, irritaiton, or abnormal discharge. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Regulatory & Marketing

Labeler Name
Good Clean Love, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
04-17-2020
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 73716-001-10 identifies a specific commercial package of 1 g in 1 blister pack of Biophresh, a human over the counter drug labeled by Good Clean Love, Inc.. This suppository is formulated for vaginal use and contains nitric acid; pulsatilla vulgaris; sepia officinalis whole; thuja occidentalis leafy twig; wood creosote 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 Good Clean Love, Inc. on April 17, 2020. The current certification is valid through December 31, 2026.

How is this Good Clean Love, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73716000110. 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)
73716-001-10
11-Digit CMS (5-4-2)
73716-0001-10

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