NDC 60681-2905 Pleo Quent

NDC Product Code 60681-2905

NDC 60681-2905-1

Package Description: 10 VIAL, GLASS in 1 CARTON > 1 mL in 1 VIAL, GLASS

NDC 60681-2905-2

Package Description: 50 VIAL, GLASS in 1 CARTON > 1 mL in 1 VIAL, GLASS

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

NDC Product Information

Pleo Quent with NDC 60681-2905 is a product labeled by Sanum Kehlbeck Gmbh & Co. Kg. The generic name of Pleo Quent 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)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)

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: 12-19-1997 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 ("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.

Pleo Quent 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 - Purpose

Oral Homeopathic Medicine10 doses, each 1 mL(.03 fl oz)

Indications

For temporary relief of congestion due to colds and minor respiratory infections.

Directions For Use

Snap off top portion of sipping container. Insert glass sipping straw.

Dosage

1-3 x weekly 1 sip

Inactive Ingredient

1 mL contains Penicillium glabrum 5X, in a base of purified saline solution.

Warning

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

Otc - Keep Out Of Reach Of Children

Keep this and all medications out of the reach of children. In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

Storage And Handling

Protect from light and heat.

Tamper Evident

Do not use this product if the glass vial is broken.

* Please review the disclaimer below.