NDC 70964-0001 Advance Plus

Carduus Marianus, Cynara Scolymus, Solidago Virgaurea, Taraxacum Officinale, Benzoicum Acidum, Berberis Vulgaris, Bryonia (alba), Cantharis, Carduus Benedictus, Ceanothus Americanus, Chelidonium Majus, Chionanthus Virginica, Cinchona Officinalis, Dioscorea Villosa, Dolichos Pruriens, Iris Versicolor, Juniperus Communis, Nux Vomica, Ptelea Trifoliata, Uricum Acidum

NDC Product Code 70964-0001

NDC Code: 70964-0001

Proprietary Name: Advance Plus 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.

Non-Proprietary Name: Carduus Marianus, Cynara Scolymus, Solidago Virgaurea, Taraxacum Officinale, Benzoicum Acidum, Berberis Vulgaris, Bryonia (alba), Cantharis, Carduus Benedictus, Ceanothus Americanus, Chelidonium Majus, Chionanthus Virginica, Cinchona Officinalis, Dioscorea Villosa, Dolichos Pruriens, Iris Versicolor, Juniperus Communis, Nux Vomica, Ptelea Trifoliata, Uricum Acidum 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.

NDC Code Structure

  • 70964 - Vitaminmed, Llc
    • 70964-0001 - Advance Plus

NDC 70964-0001-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Advance Plus with NDC 70964-0001 is a a human over the counter drug product labeled by Vitaminmed, Llc. The generic name of Advance Plus is carduus marianus, cynara scolymus, solidago virgaurea, taraxacum officinale, benzoicum acidum, berberis vulgaris, bryonia (alba), cantharis, carduus benedictus, ceanothus americanus, chelidonium majus, chionanthus virginica, cinchona officinalis, dioscorea villosa, dolichos pruriens, iris versicolor, juniperus communis, nux vomica, ptelea trifoliata, uricum acidum. The product's dosage form is spray and is administered via oral form.

Labeler Name: Vitaminmed, Llc

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug 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.

Advance Plus Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • MILK THISTLE 3 [hp_X]/mL
  • CYNARA SCOLYMUS LEAF 3 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • BENZOIC ACID 15 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • LYTTA VESICATORIA 15 [hp_X]/mL
  • CENTAUREA BENEDICTA 15 [hp_X]/mL
  • CEANOTHUS AMERICANUS LEAF 15 [hp_X]/mL
  • CHELIDONIUM MAJUS 15 [hp_X]/mL
  • CHIONANTHUS VIRGINICUS BARK 15 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 15 [hp_X]/mL
  • DIOSCOREA VILLOSA TUBER 15 [hp_X]/mL
  • MUCUNA PRURIENS FRUIT TRICHOME 15 [hp_X]/mL
  • IRIS VERSICOLOR ROOT 15 [hp_X]/mL
  • JUNIPER BERRY 15 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 15 [hp_X]/mL
  • PTELEA TRIFOLIATA BARK 15 [hp_X]/mL
  • URIC ACID 15 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

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

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Vitaminmed, Llc
Labeler Code: 70964
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 12-08-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Advance Plus Product Label Images

Advance Plus Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Carduus Marianus 3X, Cynara Scolymus 3X, Solidago Virgaurea 3X, Taraxacum Officinale 3X, 15X, Benzoicum Acidum 15X, Berberis Vulgaris 15X, Bryonia (Alba) 15X, Cantharis 15X, Carduus Benedictus 15X, Ceanothus Americanus 15X, Chelidonium Majus 15X, Chionanthus Virginica 15X, Cinchona Officinalis 15X, Dioscorea Villosa 15X, Dolichos Pruriens 15X, Iris Versicolor 15X, Juniperus Communis 15X, Nux Vomica 15X, Ptelea Trifoliata 15X, Uricum Acidum 15X.

Indications:

Formulated for liver, kidney and colon functions and for symptoms associated with toxic conditions.**These statements have not been evaluated by the Food and Drug Administration.  This product is not intended to diagnose, treat, cure, or prevent any disease.

Formulated for liver, kidney and colon functions and for symptoms associated with toxic conditions.**These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Cautions:

Do not take if you are, or suspect you are, pregnant or if you are lactating. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.STORAGE: Keep tightly closed in a cool, dry place out of reach of children.

Keep Out Of Reach Of Children:

Keep tightly closed in a cool, dry place out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Ages 12 and up, hold nozzle 1" from mouth, spray twice and swallow (ages 0 to 11, spray once) at bedtime, or use a directed by your healthcare practitioner.  Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

USP organic alcohol 20%, USP Purified water.

Questions:

Distributed by:  VitaminMed300 S Duncan Ave., Ste 263Clearwater, FL 33755www.vitaminmed.comQuestions:  800-949-7875

Packabe Label Display:

VitaminMedNDC# 70964-0001-1HomeopathicAdvance Plus1 FL OZ. 30 ML

* Please review the disclaimer below.

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