NDC 64616-093 Hcb-res
Heart, Circulatory System And Blood Booster Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64616 - Vitality Works, Inc.
- 64616-093 - Hcb-res
Product Packages
NDC Code 64616-093-02
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 64616-093?
What are Hcb-res Active Ingredients?
- GALIUM APARINE 7 [hp_X]/mL - A genus of herbaceous annual and perennial plants in the family RUBIACEAE.
- HELODERMA HORRIDUM VENOM 15 [hp_X]/mL
- KALMIA LATIFOLIA LEAF 10 [hp_X]/mL
- KEROSENE 15 [hp_X]/mL - A refined petroleum fraction used as a fuel as well as a solvent.
- MARSDENIA CONDURANGO BARK 3 [hp_X]/mL
- MILK THISTLE 7 [hp_X]/mL
- SALIX NIGRA BARK 10 [hp_X]/mL
- SEMECARPUS ANACARDIUM JUICE 5 [hp_X]/mL
- VERATRUM VIRIDE ROOT 10 [hp_X]/mL
- VERBENA OFFICINALIS 12 [hp_X]/mL
Which are Hcb-res UNII Codes?
The UNII codes for the active ingredients in this product are:
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA)
- MARSDENIA CONDURANGO BARK (UNII: R23QIR6YBA) (Active Moiety)
- GALIUM APARINE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- HELODERMA HORRIDUM VENOM (UNII: O9M1UQ4YIO)
- HELODERMA HORRIDUM VENOM (UNII: O9M1UQ4YIO) (Active Moiety)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
- KEROSENE (UNII: 1C89KKC04E)
- KEROSENE (UNII: 1C89KKC04E) (Active Moiety)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- SALIX NIGRA BARK (UNII: QU52J3A5B3) (Active Moiety)
- VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q)
- VERATRUM VIRIDE ROOT (UNII: 197B3Q7T5Q) (Active Moiety)
- VERBENA OFFICINALIS (UNII: QT8A71T9BM)
- VERBENA OFFICINALIS (UNII: QT8A71T9BM) (Active Moiety)
Which are Hcb-res 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)
- 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".