NDC 60681-6100 Pleo Chelate

NDC Product Code 60681-6100

NDC 60681-6100-1

Package Description: 1 BOTTLE, DROPPER in 1 CARTON > 100 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

Pleo Chelate with NDC 60681-6100 is a product labeled by Sanum Kehlbeck Gmbh & Co. Kg. The generic name of Pleo Chelate is . The product's dosage form is and is administered via form.

Labeler Name: Sanum Kehlbeck Gmbh & Co. Kg

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)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • HYDROGEN PEROXIDE (UNII: BBX060AN9V)
  • 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: Sanum Kehlbeck Gmbh & Co. Kg
Labeler Code: 60681
Start Marketing Date: 12-31-1996 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: 12-31-2017 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Pleo Chelate Product Label Images

Pleo Chelate 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

Indications

To optimize body minerals

Ingredients

100g solution contains 4g magnesium sulphate 2X, 4g potassium chloride 2X, 1.6g sodium chloride 2X, sodium edetate, hydrogen peroxide, water, alcohol 3% by volume.

Tamper Evident

Do not use this product if tamper-evident seal on base of bottle cap is missing or broken or if imprinted security strip on carton is torn.

Dosage

Adults: take 15 drops twice daily under tongue or diluted in water, unless otherwise recommended by your health professional.

Warning

If symptoms persist more than a few days, contact a licensed practitioner. As with any other drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.

* Please review the disclaimer below.