NDC 60512-6020 Candida Yeast Real Relief

NDC Product Code 60512-6020

NDC CODE: 60512-6020

Proprietary Name: Candida Yeast Real Relief 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.

Product Characteristics

Color(s):
WHITE (C48325)
Shape: ROUND (C48348)
Size(s):
8 MM
Score: 1

NDC Code Structure

  • 60512 - Homeolab Usa Inc

NDC 60512-6020-0

Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE

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

NDC Product Information

Candida Yeast Real Relief with NDC 60512-6020 is a product labeled by Homeolab Usa Inc. 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.

  • LACTOSE (UNII: J2B2A4N98G)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Labeler Information

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

Labeler Name: Homeolab Usa Inc
Labeler Code: 60512
Start Marketing Date: 12-14-2012 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 - 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.

Candida Yeast Real Relief Product Label Images

Candida Yeast Real Relief 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 Hpus

Baptisia tinctoria (Wild indigo) 8XBryonia (White bryony) 8XEchinacea angustifolia (Coneflower) 8XThuja occidentalis (White cedar) 8XViscum album (Mistletoe) 8X

Purpose

Fetid vaginal dischargeburning itchingmucus from vaginaitching, burning, scanty dischargepain

References

These claims have not been reviewed by the Food and Drug Administration. They are based on traditional homeopathic practice.The letters 'HPUS' indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

Uses

This homeopathic medicine helps relieve symptoms of yeast infections:- itching- burning- discharge

Otc - Stop Use

Stop use and ask a doctor if symptoms worsen or persist for more than 7 days.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

Chew tablets and let dissolve in mouth.Do not use more than directed.Do not take with food.Repeat 3 times daily and reduce with improvement or as directed by a health professional.AgeDoseAdults 2 tablets

Other Information

Store at room temperature (68 - 77F).Do not use if seal is broken or missing.

Inactive Ingredients

Lactose, magnesium stearate.

* Please review the disclaimer below.