NDC 63479-0601 F01 Angr-rls
Big Sagebrush, Bos Taurus Liver, Gallbladder, Briza Maxima, Calendula Officinalis, Ch...

Product Information

What is NDC 63479-0601?

The NDC code 63479-0601 is assigned by the FDA to the product F01 Angr-rls which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of F01 Angr-rls is big sagebrush, bos taurus liver, gallbladder, briza maxima, calendula officinalis, chamomile flower, chicory flower, garlic, english holly flower, european beech flower, forking larkspur flower, german chamomile flower, impatiens glandulifera flower, lilium tigrinum, mountain dogwood, natrum muriaticum, nux vomica, rubber rabbitbrush, vitis vinifera flower, watermelon, white willow flower, yellow star thistle. The product's dosage form is solution/ drops and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 63479-0601-1 30 ml in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code63479-0601
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
F01 Angr-rls
Non-Proprietary Name 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.
Big Sagebrush, Bos Taurus Liver, Gallbladder, Briza Maxima, Calendula Officinalis, Chamomile Flower, Chicory Flower, Garlic, English Holly Flower, European Beech Flower, Forking Larkspur Flower, German Chamomile Flower, Impatiens Glandulifera Flower, Lilium Tigrinum, Mountain Dogwood, Natrum Muriaticum, Nux Vomica, Rubber Rabbitbrush, Vitis Vinifera Flower, Watermelon, White Willow Flower, Yellow Star Thistle
Product Type 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.
Human Otc Drug
Dosage FormSolution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Sublingual - Administration beneath the tongue.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Apex Energetics Inc.
Labeler Code63479
Marketing Category 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.
UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
03-12-1996
Listing Expiration Date 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.
12-31-2023
Exclude Flag 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".
N
NDC Code Structure

What are the uses for F01 Angr-rls?


Product Packages

NDC Code 63479-0601-1

Package Description: 30 mL in 1 BOTTLE, GLASS

Product Details

What are F01 Angr-rls Active Ingredients?

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.

F01 Angr-rls Active Ingredients UNII Codes

  • ARTEMISIA TRIDENTATA WHOLE (UNII: 45E08M336T)
  • ARTEMISIA TRIDENTATA WHOLE (UNII: 45E08M336T) (Active Moiety)
  • BOS TAURUS GALLBLADDER (UNII: 9901V1E867)
  • BOS TAURUS GALLBLADDER (UNII: 9901V1E867) (Active Moiety)
  • BEEF LIVER (UNII: W8N8R55022)
  • BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
  • BRIZA MAXIMA WHOLE (UNII: 3SU44U90RR)
  • BRIZA MAXIMA WHOLE (UNII: 3SU44U90RR) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
  • CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
  • ALLIUM SATIVUM WHOLE (UNII: IIF21WT8O3)
  • ALLIUM SATIVUM WHOLE (UNII: IIF21WT8O3) (Active Moiety)
  • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W)
  • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W) (Active Moiety)
  • CONSOLIDA REGALIS FLOWER (UNII: 3O33B2269R)
  • CONSOLIDA REGALIS FLOWER (UNII: 3O33B2269R) (Active Moiety)
  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
  • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
  • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
  • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • ERICAMERIA NAUSEOSA WHOLE (UNII: H52XVP0BVB)
  • ERICAMERIA NAUSEOSA WHOLE (UNII: H52XVP0BVB) (Active Moiety)
  • VITIS VINIFERA FLOWERING TOP (UNII: 6TG3V35HTV)
  • VITIS VINIFERA FLOWERING TOP (UNII: 6TG3V35HTV) (Active Moiety)
  • WATERMELON (UNII: 231473QB6R)
  • WATERMELON (UNII: 231473QB6R) (Active Moiety)
  • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R)
  • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (Active Moiety)
  • CENTAUREA SOLSTITIALIS WHOLE (UNII: 59CH355QGQ)
  • CENTAUREA SOLSTITIALIS WHOLE (UNII: 59CH355QGQ) (Active Moiety)
  • MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02)
  • MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02) (Active Moiety)
  • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
  • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
  • CHAMOMILE (UNII: FGL3685T2X)
  • CHAMOMILE (UNII: FGL3685T2X) (Active Moiety)
  • CORNUS NUTTALLII WHOLE (UNII: F34859WS62)
  • CORNUS NUTTALLII WHOLE (UNII: F34859WS62) (Active Moiety)

F01 Angr-rls 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.

Pharmacologic Class(es)

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F01 Angr-rls Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



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