NDC 60681-1303 Pleo Lari

  1. Labeler Index
  2. Sanum Kehlbeck Gmbh & Co. Kg
  3. NDC: 60681-1303 Pleo Lari

NDC Product Code 60681-1303

NDC CODE: 60681-1303

Proprietary Name: Pleo Lari 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 60681-1303-1

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

NDC 60681-1303-2

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 Lari with NDC 60681-1303 is a product labeled by Sanum Kehlbeck Gmbh & Co. Kg. The generic name of Pleo Lari 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: 01-19-1998 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 Lari Product Label Images

Pleo Lari 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

For temporary relief of pain associated with arthritis.

Directions For Use

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

Dosage

1 SIP, twice weekly.

Ingredients

1 mL contains Laricifomes officinalis 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.

Tamper Evident

Do not use this product if the glass vial is broken or if imprinted security strip on carton is torn.

* Please review the disclaimer below.