NDC 62713-930 Candicide

NDC Product Code 62713-930

NDC CODE: 62713-930

Proprietary Name: Candicide 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.

NDC Code Structure

  • 62713 - Meditrend, Inc. Dba Progena Professional Formulations

NDC 62713-930-01

Package Description: 30 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

Candicide with NDC 62713-930 is a product labeled by Meditrend, Inc. Dba Progena Professional Formulations. The product's dosage form is and is administered via form.

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.

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

Product Labeler Information

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

Labeler Name: Meditrend, Inc. Dba Progena Professional Formulations
Labeler Code: 62713
Start Marketing Date: 10-10-2014 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 - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Candicide Product Label Images

Candicide 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

Otc - Active Ingredient

Active Ingredients (HPUS): Baptisia Tinctoria 3X, Borax 30X,


Calcarea Carbonica 30X, Candida Albicans (12X, 30x, 60x, 100x, 500x), Kreosotum 30X,


Lycopodium Clavatum 30X, Nux Vomica 30X, Phosphoricum


Acidum 30X, Pulsatilla 30X, Sepia 30X.

Otc - Purpose

Purpose:


Support for the Treatment of Symptoms Associated with


Candida Albicans.

Indications & Usage

Use: This product is a Homeopathic Dilution, formulated to help


improve the body’s immunity in the treatment of diagnosed


Candida Albicans.

Warnings

Warnings: Use only as directed.

Otc - Stop Use

Stop use and ask a doctor if symptoms worsen or do not

improve after 5 days.

Otc - Do Not Use

Do not use this product, if you have abdominal pain, fever, or foul

smelling discharge. You may have a condition which is more serious.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, consult a health professional

before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of overdose, get medical

help or contact a Poison Control Center right away.

Dosage & Administration

Directions:Adults (12 and Older) take 15 drops under the


tongue three times daily.


Children (11 and Younger) take 10 drops


under the tongue three times daily or as directed by your health


care professional.


Consult a Physician for use in children under


12 years of age.


Not Recommended for Children Under 2


Years of Age.

Other Safety Information

Other Information: Do not use if TAMPER EVIDENT seal


around neck of bottle is missing or broken.

Inactive Ingredient

Inactive Ingredients: Demineralized water and 25% USP Ethanol.

* Please review the disclaimer below.