NDC Package 61096-2034-1 Woman Power

Agnus,Aralia Quin,Arnica,Damiana,Lactuca,Nat Mur,Onosmodium - 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:
61096-2034-1
Package Description:
1 BOTTLE, SPRAY in 1 CARTON / 41 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Woman Power
Non-Proprietary Name:
Agnus, Aralia Quin, Arnica, Damiana, Lactuca, Nat Mur, Onosmodium Virginianum, Oophorinum, Phosphoricum Ac, Pituitarum Posterium, Salix Nig, Sepia, Thuja Occ
Substance Name:
American Ginseng; Arnica Montana; Chaste Tree; Lactuca Virosa; Onosmodium Virginianum Whole; Phosphoric Acid; Salix Nigra Bark; Sepia Officinalis Juice; Sodium Chloride; Sus Scrofa Ovary; Sus Scrofa Pituitary Gland; Thuja Occidentalis Leafy Twig; Turnera Diffusa Leafy Twig
Usage Information:
Temporarily relieves the symptoms of low female energy, including:° decreased sexual desire° low physical energy° irritability° "the blues"° natural° gluten & lactose free° no artificial flavors or colors° no known negative side effects° no known negative drug interactions
11-Digit NDC Billing Format:
61096203401
Product Type:
Human Otc Drug
Labeler Name:
Eight And Company L.l.c
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(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    03-25-2019
    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 61096-2034-1?

    The NDC Packaged Code 61096-2034-1 is assigned to a package of 1 bottle, spray in 1 carton / 41 ml in 1 bottle, spray of Woman Power, a human over the counter drug labeled by Eight And Company L.l.c. The product's dosage form is liquid and is administered via oral form.

    Is NDC 61096-2034 included in the NDC Directory?

    Yes, Woman Power with product code 61096-2034 is active and included in the NDC Directory. The product was first marketed by Eight And Company L.l.c on March 25, 2019 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 61096-2034-1?

    The 11-digit format is 61096203401. 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 5-4-1 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
    5-4-161096-2034-15-4-261096-2034-01