NDC 63479-0106 A06 Revitalization
Avena Sativa,Bone Marrow Suis,Bos Taurus Adrenal Gland,Bos Taurus Artery,Bos Taurus - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63479-0106?
What are the uses for A06 Revitalization?
What are A06 Revitalization Active Ingredients?
- AVENA SATIVA FLOWERING TOP 4 [hp_X]/mL
- BEEF KIDNEY 7 [hp_C]/mL
- BEEF LIVER 7 [hp_C]/mL
- BOS TAURUS ADRENAL GLAND 7 [hp_C]/mL
- BOS TAURUS ARTERY 7 [hp_C]/mL
- BOS TAURUS COLON 7 [hp_C]/mL
- BOS TAURUS LYMPH VESSEL 7 [hp_C]/mL
- BOS TAURUS PANCREAS 7 [hp_C]/mL
- BOS TAURUS PITUITARY GLAND, POSTERIOR 7 [hp_C]/mL
- BOS TAURUS PLACENTA 15 [hp_C]/mL
- BOS TAURUS SKIN 7 [hp_C]/mL
- BOS TAURUS THYMUS 7 [hp_C]/mL
- GENTIANA LUTEA ROOT 6 [hp_X]/mL
- GLYCYRRHIZA GLABRA 6 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 9 [hp_X]/mL
- HYDROFLUORIC ACID 30 [hp_X]/mL - Hydrofluoric acid. A solution of hydrogen fluoride in water. It is a colorless fuming liquid which can cause painful burns.
- POTASSIUM PHOSPHATE, DIBASIC 10 [hp_X]/mL
- PROCAINE 8 [hp_X]/mL - A local anesthetic of the ester type that has a slow onset and a short duration of action. It is mainly used for infiltration anesthesia, peripheral nerve block, and spinal block. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1016).
- SUS SCROFA BONE MARROW 7 [hp_C]/mL
- SUS SCROFA SPLEEN 7 [hp_C]/mL
Which are A06 Revitalization UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y)
- SUS SCROFA SPLEEN (UNII: 92AMN5J79Y) (Active Moiety)
- BEEF KIDNEY (UNII: 5HOC10FSIC)
- BEEF KIDNEY (UNII: 5HOC10FSIC) (Active Moiety)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (Active Moiety)
- BOS TAURUS PLACENTA (UNII: 83AL37E3A7)
- BOS TAURUS PLACENTA (UNII: 83AL37E3A7) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- PROCAINE (UNII: 4Z8Y51M438)
- PROCAINE (UNII: 4Z8Y51M438) (Active Moiety)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D)
- BOS TAURUS PANCREAS (UNII: 1M529TNT1D) (Active Moiety)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND, POSTERIOR (UNII: 7JM57I419K) (Active Moiety)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8)
- SUS SCROFA BONE MARROW (UNII: VP2CN2G7Y8) (Active Moiety)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29)
- BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (Active Moiety)
- BOS TAURUS ARTERY (UNII: R2M88A4HSI)
- BOS TAURUS ARTERY (UNII: R2M88A4HSI) (Active Moiety)
- BOS TAURUS COLON (UNII: 8PD5L21RYS)
- BOS TAURUS COLON (UNII: 8PD5L21RYS) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- BOS TAURUS SKIN (UNII: 7J12CD6O9L)
- BOS TAURUS SKIN (UNII: 7J12CD6O9L) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
Which are A06 Revitalization 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)
Which are the Pharmacologic Classes for A06 Revitalization?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Cells, Epidermal - [EXT]
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Meat Proteins - [EXT]
- Non-Standardized Animal Skin Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
* 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".