NDC 63479-0618 F18 Rlxtn

Apricot,Chamomile,Coffea Arabica,Coffea Cruda,Comfrey,Crimson Monkey,Date - View Dosage, Usage, Ingredients, Routes, UNII

Product Information
Product Packages
What is NDC 63479-0618?
F18 Rlxtn Uses
Active Ingredients
Active Ingredients UNII Codes
Inactive Ingredients UNII Codes
Pharmacologic Classes

Product Information

NDC Product Code:

63479-0618

Proprietary Name:

F18 Rlxtn

Non-Proprietary Name: [1]

Apricot, Chamomile, Coffea Arabica, Coffea Cruda, Comfrey, Crimson Monkey, Date Palm, Dill, English Elm Ing Twig, European Aspen, Filaree, Golden Eardrops, Horse Chestnut, Humulus Lupulus, Hypericum Perforatum, Hypericum Perforatum Flower, Impatiens Glandulifera, Magnesia Phosphorica, Mexican Pink, Mimulus Guttatus, Nux Vomica, Oregon Grapeholly, Passiflora Incarnata, Scutellaria Lateriflora, Sweet Chestnut, Verbena Officinalis, Watermelon, Yerba Santa, Zincum Valerianicum

Substance Name: [2]

Aesculus Hippocastanum Flower; Anethum Graveolens Whole; Arabica Coffee Bean; Berberis Aquifolium Whole; Calochortus Gunnisonii Whole; Castanea Sativa Flower; Coffea Arabica Whole; Ehrendorferia Chrysantha Whole; Eriodictyon Californicum Flowering Top; Erodium Cicutarium; Erythranthe Cardinalis Whole; Hops; Hypericum Perforatum; Hypericum Perforatum Flower; Impatiens Glandulifera Flower; Magnesium Phosphate, Dibasic Trihydrate; Matricaria Recutita Flowering Top; Mimulus Guttatus Flowering Top; Passiflora Incarnata Flowering Top; Phoenix Dactylifera Whole; Populus Tremula Flowering Top; Prunus Armeniaca Whole; Scutellaria Lateriflora Whole; Silene Laciniata Whole; Strychnos Nux-vomica Seed; Symphytum Officinale Whole; Ulmus Procera Flowering Twig; Verbena Officinalis Flowering Top; Watermelon; Zinc Valerate Dihydrate

NDC Directory Status:

Human Otc Drug

Product Type: [3]

ACTIVE PRODUCT INCLUDED in the NDC Directory

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 Name: [5]

Apex Energetics Inc.

Labeler Code:

63479

Product Label ID:

bd1d02fd-9915-46d3-e053-2a95a90a39be

Marketing Category: [8]

UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Start Marketing Date: [9]

03-12-1996

Listing Expiration Date: [11]

12-31-2025

Exclude Flag: [12]

Code Structure:

63479 - Apex Energetics Inc.
- 63479-0618 - F18
  - 63479-0618-1

Code Navigator:

Product Packages

NDC Code 63479-0618-1

Package Description: 30 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 63479-0618?

The NDC code 63479-0618 is assigned by the FDA to the product F18 Rlxtn which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of F18 Rlxtn is apricot, chamomile, coffea arabica, coffea cruda, comfrey, crimson monkey, date palm, dill, english elm ing twig, european aspen, filaree, golden eardrops, horse chestnut, humulus lupulus, hypericum perforatum, hypericum perforatum flower, impatiens glandulifera, magnesia phosphorica, mexican pink, mimulus guttatus, nux vomica, oregon grapeholly, passiflora incarnata, scutellaria lateriflora, sweet chestnut, verbena officinalis, watermelon, yerba santa, zincum valerianicum. 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 63479-0618-1 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 and RxNorm crosswalk.

What are the uses for F18 Rlxtn?

Adults & children ages 12 years and over: Take 10 drops under the tongue 2-3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

What are F18 Rlxtn 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.

Which are F18 Rlxtn UNII Codes?

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

IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
SILENE LACINIATA WHOLE (UNII: 565ZR7YWT0)
SILENE LACINIATA WHOLE (UNII: 565ZR7YWT0) (Active Moiety)
HYPERICUM PERFORATUM FLOWER (UNII: A6V4CUE7PV)
HYPERICUM PERFORATUM FLOWER (UNII: A6V4CUE7PV) (Active Moiety)
ANETHUM GRAVEOLENS WHOLE (UNII: BWN6849791)
ANETHUM GRAVEOLENS WHOLE (UNII: BWN6849791) (Active Moiety)
AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
PRUNUS ARMENIACA WHOLE (UNII: 10TCS27K2T)
PRUNUS ARMENIACA WHOLE (UNII: 10TCS27K2T) (Active Moiety)
ERYTHRANTHE CARDINALIS WHOLE (UNII: 4MGZ04S7LT)
ERYTHRANTHE CARDINALIS WHOLE (UNII: 4MGZ04S7LT) (Active Moiety)
SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)
SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y) (Active Moiety)
MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02)
MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02) (Active Moiety)
COFFEA ARABICA WHOLE (UNII: 90J8498ESR)
COFFEA ARABICA WHOLE (UNII: 90J8498ESR) (Active Moiety)
ARABICA COFFEE BEAN (UNII: 3SW678MX72)
ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
PHOENIX DACTYLIFERA WHOLE (UNII: 8QI9RWU9M1)
PHOENIX DACTYLIFERA WHOLE (UNII: 8QI9RWU9M1) (Active Moiety)
EHRENDORFERIA CHRYSANTHA WHOLE (UNII: 68HKD4QMJR)
EHRENDORFERIA CHRYSANTHA WHOLE (UNII: 68HKD4QMJR) (Active Moiety)
CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3)
CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3) (Active Moiety)
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
BERBERIS AQUIFOLIUM WHOLE (UNII: J4WG1JVR05)
BERBERIS AQUIFOLIUM WHOLE (UNII: J4WG1JVR05) (Active Moiety)
PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)
VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ)
VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ) (Active Moiety)
SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC)
SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC) (Active Moiety)
WATERMELON (UNII: 231473QB6R)
WATERMELON (UNII: 231473QB6R) (Active Moiety)
ERIODICTYON CALIFORNICUM FLOWERING TOP (UNII: HKE3DK7994)
ERIODICTYON CALIFORNICUM FLOWERING TOP (UNII: HKE3DK7994) (Active Moiety)
ZINC VALERATE DIHYDRATE (UNII: MN0RX54EQA)
VALERIC ACID (UNII: GZK92PJM7B) (Active Moiety)
ULMUS PROCERA FLOWERING TWIG (UNII: J3O020I532)
ULMUS PROCERA FLOWERING TWIG (UNII: J3O020I532) (Active Moiety)
POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ)
POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ) (Active Moiety)
ERODIUM CICUTARIUM (UNII: FJL3XFK3N8)
ERODIUM CICUTARIUM (UNII: FJL3XFK3N8) (Active Moiety)
CALOCHORTUS GUNNISONII WHOLE (UNII: H4ORZ75P00)
CALOCHORTUS GUNNISONII WHOLE (UNII: H4ORZ75P00) (Active Moiety)
HOPS (UNII: 01G73H6H83)
HOPS (UNII: 01G73H6H83) (Active Moiety)
MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU)
MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU) (Active Moiety)

Which are F18 Rlxtn 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:

WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Which are the Pharmacologic Classes for F18 Rlxtn?

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.

* Please review the disclaimer below.

Product Footnotes

[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".

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