Female Stimulant Liquid
NDC Package 43742-1507-1

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

Package Information

Female Stimulant (lilium tigrinum, bovista, cypripedium pubescens, hydrastis canadensis, petroselinum sativum, aquilegia vulgaris, funiculus umbilicalis suis, glandula suprarenalis suis, heart (suis), kreosotum, oophorinum (suis), uterus (suis), folliculinum, lachesis mutus, magnesia phosphorica, mercurius solubilis, sepia, pineal gland (suis), hypophysis suis, aconiticum acidum cis-, apis venenum purum, estradiol, progesterone, testosterone, placenta totalis suis, faecalis (alkaligenes), mutabile bacillus (bach)) liquids is for temporary relief of symptoms related to female hormonal problems such as fatigue and low energy.****These statements are based upon traditional homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-1507.

Identification & Billing

NDC Package Code
43742-1507-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43742-1507
11-Digit Billing Format
43742150701

Clinical Specifications

Proprietary Name
Female Stimulant
Non-Proprietary Name
Lilium Tigrinum, Bovista, Cypripedium Pubescens, Hydrastis Canadensis, Petroselinum Sativum, Aquilegia Vulgaris, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Heart (suis), Kreosotum, Oophorinum (suis), Uterus (suis), Folliculinum, Lachesis Mutus, Magnesia Phosphorica, Mercurius Solubilis, Sepia, Pineal Gland (suis), Hypophysis Suis, Aconiticum Acidum Cis-, Apis Venenum Purum, Estradiol, Progesterone, Testosterone, Placenta Totalis Suis, Faecalis (alkaligenes), Mutabile Bacillus (bach)
Substance Name
Aconitic Acid, (z)-; Alcaligenes Faecalis; Apis Mellifera Venom; Aquilegia Vulgaris; Cypripedium Parviflorum Var. Pubescens Root; Escherichia Coli; Estradiol; Estrone; Goldenseal; Lachesis Muta Venom; Lilium Lancifolium Whole Flowering; Lycoperdon Utriforme Fruiting Body; Magnesium Phosphate, Dibasic Trihydrate; Mercurius Solubilis; Petroselinum Crispum Whole; Pork Heart; Progesterone; Sepia Officinalis Juice; Sus Scrofa Adrenal Gland; Sus Scrofa Ovary; Sus Scrofa Pineal Gland; Sus Scrofa Pituitary Gland; Sus Scrofa Placenta; Sus Scrofa Umbilical Cord; Sus Scrofa Uterus; Testosterone; Wood Creosote
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For temporary relief of symptoms related to female hormonal problems such as fatigue and low energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to female hormonal problems such as fatigue and low energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.
DEA Schedule
Schedule III (CIII) Substances

Regulatory & Marketing

Labeler Name
Deseret Biologicals, 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
08-20-2019
End Marketing Date
01-02-2030
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 43742-1507-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Female Stimulant, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains aconitic acid, (z)-; alcaligenes faecalis; apis mellifera venom; aquilegia vulgaris; cypripedium parviflorum var. pubescens root; escherichia coli; estradiol; estrone; goldenseal; lachesis muta venom; lilium lancifolium whole flowering; lycoperdon utriforme fruiting body; magnesium phosphate, dibasic trihydrate; mercurius solubilis; petroselinum crispum whole; pork heart; progesterone; sepia officinalis juice; sus scrofa adrenal gland; sus scrofa ovary; sus scrofa pineal gland; sus scrofa pituitary gland; sus scrofa placenta; sus scrofa umbilical cord; sus scrofa uterus; testosterone; 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 Deseret Biologicals, Inc. on August 20, 2019.

How is this Deseret Biologicals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742150701. 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 (5-4-1)
43742-1507-1
11-Digit CMS (5-4-2)
43742-1507-01

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