NDC 60681-5302 Pleo Ut

NDC Product Code 60681-5302

NDC 60681-5302-2

Package Description: 1 BLISTER PACK in 1 CARTON > 5 CAPSULE in 1 BLISTER PACK

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

NDC Product Information

Pleo Ut with NDC 60681-5302 is a product labeled by Sanum Kehlbeck Gmbh & Co. Kg. The generic name of Pleo Ut 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.

  • LACTOSE (UNII: J2B2A4N98G)
  • HYPROMELLOSE (UNII: 3NXW29V3WO)

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: 03-19-1996 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 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 Ut Product Label Images

Pleo Ut 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 pain relief of swollen lymph glands.

Ingredients

1 capsule contains 330 mg Bacillus subtilis 4X in a base of lactose.

Other Components

Capsule shells consist of Hypromellose (HPMC).

Dosage

1–2 capsules weekly, one capsule either before breakfast or at bedtime.

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 taking this product. 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. Protect from light and heat.

Tamper Evident

Do not use this product if shrink-wrap is missing from the carton or the imprinted blister foil is broken.

* Please review the disclaimer below.