NDC 43965-0001 Compre Tox

NDC Product Code 43965-0001

NDC 43965-0001-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Compre Tox with NDC 43965-0001 is a product labeled by Kevin Sullivan Navillus. The generic name of Compre Tox is . The product's dosage form is and is administered via form.

Labeler Name: Kevin Sullivan Navillus

Dosage Form: -

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.

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)

Product Labeler Information

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

Labeler Name: Kevin Sullivan Navillus
Labeler Code: 43965
Start Marketing Date: 09-28-2012 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: 12-31-2019 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: I 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.

Compre Tox Product Label Images

Compre Tox 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

Eriodictyon Californicum 3X, Hamamelis Virginiana 3X, Nymphaea Odorata 3X, Plantago Major 3X, Xanthoxylum Fraxineum 3X, Xerophyllum Asphodeloides 3X, Yucca Filamentosa 3X, Zingiber Officinale 3X.

Indications

For temporary relief of symptoms from general toxin exposure.

Warnings

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away. If pregnant or breast-feeding, seek advice of a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

Directions

10 drops orally, 2 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients

Demineralized Water, 25% Ethanol.

Keep Out Of Reach Of Children

In case of overdose, contact physician or Poison Control Center right away.

Indications And Usage

For temporary relief of symptoms from general toxin exposure.

Questions

MFD. FOR:Navillus4217 New Hope Meadow RoadHeritage, TN 37076

* Please review the disclaimer below.