NDC 83027-0005 Femmepap
Thuja Occidentalis,Nitricum Acidum,Causticum,Sabina,X-ray,Antimonium Sulphuratum,Human - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 83027-0005?
What are the uses for Femmepap?
What are Femmepap Active Ingredients?
- ALCOHOL, X-RAY EXPOSED (1000 RAD) 15 [hp_X]/mL
- ANTIMONY PENTASULFIDE 18 [hp_X]/mL
- CAUSTICUM 6 [hp_X]/mL
- HUMAN ADENOVIRUS E SEROTYPE 4 STRAIN CL-68578 ANTIGEN 20 [hp_C]/mL
- HUMAN PAPILLOMAVIRUS 20 [hp_X]/mL
- JUNIPERUS SABINA LEAFY TWIG 6 [hp_X]/mL
- NITRIC ACID 6 [hp_X]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
- THUJA OCCIDENTALIS LEAFY TWIG 4 [hp_X]/mL
Which are Femmepap UNII Codes?
The UNII codes for the active ingredients in this product are:
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1)
- JUNIPERUS SABINA LEAFY TWIG (UNII: Z5BEX9K2G1) (Active Moiety)
- ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P)
- ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (Active Moiety)
- ANTIMONY PENTASULFIDE (UNII: 1433F1I86N)
- ANTIMONY PENTASULFIDE (UNII: 1433F1I86N) (Active Moiety)
- HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J)
- HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J) (Active Moiety)
- HUMAN ADENOVIRUS E SEROTYPE 4 STRAIN CL-68578 ANTIGEN (UNII: FKD3DUK39I)
- HUMAN ADENOVIRUS E SEROTYPE 4 STRAIN CL-68578 (UNII: FKD3DUK39I) (Active Moiety)
Which are Femmepap Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Femmepap?
- 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]
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".