F01 Solution/ Drops
NDC 63479-0601

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0601?
  4. F01 Angr-rls Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

F01 (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) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Apex Energetics Inc.. This medication is typically used as a allergens [cs]. It is supplied as a solution/ drops for sublingual administration. This product entry covers the primary NDC 63479-0601 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
63479-0601
Proprietary Name:
F01 Angr-rls
Non-Proprietary Name: [1]
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
Substance Name: [2]
Allium Sativum Whole; Artemisia Tridentata Whole; Beef Liver; Bos Taurus Gallbladder; Briza Maxima Whole; Calendula Officinalis Flowering Top; Centaurea Solstitialis Whole; Chamomile; Cichorium Intybus Flower; Consolida Regalis Flower; Cornus Nuttallii Whole; Ericameria Nauseosa Whole; Fagus Sylvatica Flowering Top; Ilex Aquifolium Flowering Top; Impatiens Glandulifera Flower; Lilium Lancifolium Whole Flowering; Matricaria Recutita Flowering Top; Salix Alba Flowering Top; Sodium Chloride; Strychnos Nux-vomica Seed; Vitis Vinifera Flowering Top; Watermelon
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
Sublingual - Administration beneath the tongue.

Labeler & Regulatory Data

Labeler Name: [5]
Apex Energetics Inc.
Labeler Code:
63479
Product Label ID:
bd0b2eab-b6eb-19ce-e053-2a95a90aebe6
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
03-12-1996
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 63479-0601?

The NDC code 63479-0601 is assigned by the FDA to the product F01 Angr-rls. It is commonly known by its generic name, 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. This pharmaceutical product is labeled by Apex Energetics Inc. and is currently categorized as listed product. The medication is a solution/ drops administered via sublingual route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63479-0601-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Adults & children ages 12 years and over: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

What are Active Ingredients of this product?

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.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • 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)

Which are the Inactive Ingredients associated 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:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".