NDC 63479-0507 E07 Type A Balance
Aconitum Napellus,Aralia Quinquefolia,Chininum Arsenicosum,Coffea Cruda,Colchicum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63479-0507?
What are the uses for E07 Type A Balance?
What are E07 Type A Balance Active Ingredients?
- ACONITUM NAPELLUS 8 [hp_X]/mL - A plant genus of the family RANUNCULACEAE. Members contain a number of diterpenoid alkaloids including: aconitans, hypaconitine, ACONITINE, jesaconitine, ignavine, napelline, and mesaconitine. The common name of Wolfbane is similar to the common name for ARNICA.
- AMERICAN GINSENG 15 [hp_X]/mL
- ARABICA COFFEE BEAN 12 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 12 [hp_X]/mL
- CRATAEGUS LAEVIGATA FRUIT 4 [hp_X]/mL
- ECHINACEA PURPUREA 3 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- ESCHSCHOLZIA CALIFORNICA 1 [hp_X]/mL - A plant genus of the family PAPAVERACEAE that contains benzo[c]phenanthridine alkaloids.
- GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
- HOPS 1 [hp_X]/mL
- LYCOPUS VIRGINICUS 1 [hp_X]/mL - A plant genus of the family LAMIACEAE that contains rosmarinic acid and isopimarane diterpenoids and has been used in folk medicine for HYPERTHYROIDISM.
- PASSIFLORA INCARNATA TOP 1 [hp_X]/mL
- QUININE ARSENITE 6 [hp_X]/mL
- SCUTELLARIA LATERIFLORA WHOLE 1 [hp_X]/mL
- STRYCHNINE PHOSPHATE DIHYDRATE 12 [hp_X]/mL
- STRYCHNOS IGNATII SEED 8 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- THYROID, UNSPECIFIED 9 [hp_C]/mL
- VISCUM ALBUM FRUITING TOP 3 [hp_X]/mL
Which are E07 Type A Balance UNII Codes?
The UNII codes for the active ingredients in this product are:
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
- STRYCHNINE PHOSPHATE DIHYDRATE (UNII: TD67SYY51D)
- STRYCHNINE (UNII: H9Y79VD43J) (Active Moiety)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- ESCHSCHOLZIA CALIFORNICA (UNII: 9315HN272X)
- ESCHSCHOLZIA CALIFORNICA (UNII: 9315HN272X) (Active Moiety)
- HOPS (UNII: 01G73H6H83)
- HOPS (UNII: 01G73H6H83) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- LYCOPUS VIRGINICUS (UNII: TWH5125Q6F)
- LYCOPUS VIRGINICUS (UNII: TWH5125Q6F) (Active Moiety)
- PASSIFLORA INCARNATA TOP (UNII: CLF5YFS11O)
- PASSIFLORA INCARNATA TOP (UNII: CLF5YFS11O) (Active Moiety)
- SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC)
- SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC) (Active Moiety)
- CRATAEGUS LAEVIGATA FRUIT (UNII: D5RZ7MF1YF)
- CRATAEGUS LAEVIGATA FRUIT (UNII: D5RZ7MF1YF) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
- QUININE ARSENITE (UNII: 42QO5P0NLM)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- ARSENITE ION (UNII: N5509X556J) (Active Moiety)
- AMERICAN GINSENG (UNII: 8W75VCV53Q)
- AMERICAN GINSENG (UNII: 8W75VCV53Q) (Active Moiety)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
Which are E07 Type A Balance 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 E07 Type A Balance?
- Allergens - [CS]
- Allergens - [CS]
- Antimalarial - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
* 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".