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  5. NDC Package Code: 73716-001-10 Biophresh

NDC Package 73716-001-10 Biophresh

Kreosotum 6c,Nitricum Acidum 6c,Thuja Occidentalis 6c,Pulsatilla Vulgaris 6c,Sepia - 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:
73716-001-10
Package Description:
1 g in 1 BLISTER PACK
Product Code:
73716-001
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
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.
11-Digit NDC Billing Format:
73716000110
Product Type:
Human Otc Drug
Labeler Name:
Good Clean Love, Inc.
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(s):
  • Vaginal - Administration into the vagina.
    • Active Ingredient(s):
  • NITRIC ACID 6 [hp_C]/g
  • PULSATILLA VULGARIS 6 [hp_C]/g
  • SEPIA OFFICINALIS WHOLE 6 [hp_C]/g
  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_C]/g
  • WOOD CREOSOTE 6 [hp_C]/g
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    04-17-2020
    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 73716-001-10?

    The NDC Packaged Code 73716-001-10 is assigned to a package of 1 g in 1 blister pack of Biophresh, a human over the counter drug labeled by Good Clean Love, Inc.. The product's dosage form is suppository and is administered via vaginal form.

    Is NDC 73716-001 included in the NDC Directory?

    Yes, Biophresh with product code 73716-001 is active and included in the NDC Directory. The product was first marketed by Good Clean Love, Inc. on April 17, 2020 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 73716-001-10?

    The 11-digit format is 73716000110. 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
    5-3-273716-001-105-4-273716-0001-10