NDC 60681-2810 Pleo Poly T

NDC Product Code 60681-2810

NDC 60681-2810-1

Package Description: 1 BOTTLE, DROPPER in 1 CARTON > 10 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 Poly T with NDC 60681-2810 is a product labeled by Sanum Kehlbeck Gmbh & Co. Kg. The generic name of Pleo Poly T is . The product's dosage form is and is administered via form.

Labeler Name: Sanum Kehlbeck Gmbh & Co. Kg

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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)

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: 04-07-1999 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 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 Poly T 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

Headache and arthritis/rheumatism pain.

Dosage

Unless otherwise prescribed, apply 5-10 drops into the bend of the elbow and rub in three times daily.

Otc - Ask Doctor

If symptoms persist more than a few days, contact a licensed practitioner.

Otc - Pregnancy Or Breast Feeding

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 other medications out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Otc - When Using

Protect from light and heat.

Ingredients

10 mL aqueous dilution contains: antitoxins and antigens 9X of Mycobacterium tuberculosis typus humanus, brevis, and bovinus; Diplococcus pneumoniae, Streptococcus mucosus.

Inactive Ingredient

Inactive Ingredient water

Tamper Evident

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

Other

Made in GermanyDistributed by:SANUM USA Corp.1465 Slater RoadFerndale, WA 98248Manufactured by:Sanum-KehlbeckGmbH & Co. KGHoya, GermanyRev. 05/2010

* Please review the disclaimer below.