NDC 27281-039 Vivacity
Alfalfa,Arnica Montana,Avena Sativa,Galium Aparine,Hepar Suis,Hypericum Perforatum,Korean - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 27281-039?
What are Vivacity Active Ingredients?
- ALFALFA 2 [hp_X]/30mL
- ARNICA MONTANA 3 [hp_X]/30mL
- ASIAN GINSENG 2 [hp_X]/30mL
- AVENA SATIVA FLOWERING TOP 2 [hp_X]/30mL
- CERVUS ELAPHUS HORN OIL 6 [hp_X]/30mL
- GALIUM APARINE 3 [hp_X]/30mL - A genus of herbaceous annual and perennial plants in the family RUBIACEAE.
- HYPERICUM PERFORATUM 200 [hp_C]/30mL
- PORK LIVER 6 [hp_X]/30mL
- SACCHAROMYCES CEREVISIAE RNA 6 [hp_X]/30mL
- SUS SCROFA PITUITARY GLAND 8 [hp_X]/30mL
- THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_C]/30mL
- TOXICODENDRON PUBESCENS LEAF 200 [hp_C]/30mL
Which are Vivacity UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALFALFA (UNII: DJO934BRBD)
- ALFALFA (UNII: DJO934BRBD) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- GALIUM APARINE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
- CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12)
- CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX)
- SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Vivacity 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:
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
* 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".