NDC 69758-325 Hemotreat

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69758-325
Proprietary Name:
Hemotreat
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Global Treat Srl
Labeler Code:
69758
Start Marketing Date: [9]
12-20-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69758-325-55

Package Description: 5 POUCH in 1 BOX / 5 mL in 1 POUCH

Product Details

What is NDC 69758-325?

The NDC code 69758-325 is assigned by the FDA to the product Hemotreat which is product labeled by Global Treat Srl. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69758-325-55 5 pouch in 1 box / 5 ml in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Hemotreat?

AdultsWhen practical, cleanse the affected area with mild soap and warm waterGently dry by patting or blotting with toilet tissue or a soft cloth before application of ointmentWith the help of the index finger, apply a generous layer of ointmentFor optimal results apply at least 2 times a day, morning and evening, for 5-7 consecutive days. Spread on to the affected area, generally on the exterior of the anus and in the vicinity of the anal orifice. Product should stay on affected area for several hours. Reapply if bathroom trip results in product removal.

Which are Hemotreat UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Hemotreat Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".