NDC Package 83027-0005-1 Femmepap

Thuja Occidentalis,Nitricum Acidum,Causticum,Sabina,X-ray,Antimonium Sulphuratum,Human - 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:
83027-0005-1
Package Description:
60 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Femmepap
Non-Proprietary Name:
Thuja Occidentalis, Nitricum Acidum, Causticum, Sabina, X-ray, Antimonium Sulphuratum, Human Papilloma Nosode, Adenoviren Nosode
Substance Name:
Alcohol, X-ray Exposed (1000 Rad); Antimony Pentasulfide; Causticum; Human Adenovirus E Serotype 4 Strain Cl-68578 Antigen; Human Papillomavirus; Juniperus Sabina Leafy Twig; Nitric Acid; Thuja Occidentalis Leafy Twig
Usage Information:
Adults: 3 to 5 sprays three times daily. Also spray directly on affected area 3 times daily and let air dry. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
83027000501
Product Type:
Human Otc Drug
Labeler Name:
Nutritional Specialties, Inc.
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Pharmacologic Class(es):
  • Actively Acquired Immunity - [PE] (Physiologic Effect)
  • Live Human Adenovirus Type 4 Vaccine - [EPC] (Established Pharmacologic Class)
  • Vaccines, Adenovirus - [Chemical/Ingredient]
  • Vaccines, Live, Unattenuated - [Chemical/Ingredient]
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    03-27-2023
    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 83027-0005-1?

    The NDC Packaged Code 83027-0005-1 is assigned to a package of 60 ml in 1 bottle, spray of Femmepap, a human over the counter drug labeled by Nutritional Specialties, Inc.. The product's dosage form is spray and is administered via oral form.

    Is NDC 83027-0005 included in the NDC Directory?

    Yes, Femmepap with product code 83027-0005 is active and included in the NDC Directory. The product was first marketed by Nutritional Specialties, Inc. on March 27, 2023 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 83027-0005-1?

    The 11-digit format is 83027000501. 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
    5-4-183027-0005-15-4-283027-0005-01