NDC 55739-1022 Perineze Triple Dye
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55739 - Peace Medical Inc.
- 55739-1022 - Perineze Triple Dye
Product Packages
NDC Code 55739-1022-3
Package Description: 250 AMPULE in 1 BOX / .61 mL in 1 AMPULE
Product Details
What is NDC 55739-1022?
What are the uses for Perineze Triple Dye?
Which are Perineze Triple Dye UNII Codes?
The UNII codes for the active ingredients in this product are:
- BRILLIANT GREEN (UNII: G0L543D370)
- BRILLIANT GREEN (UNII: G0L543D370) (Active Moiety)
- PROFLAVINE HEMISULFATE (UNII: 27V8M747VB)
- PROFLAVINE HEMISULFATE (UNII: 27V8M747VB) (Active Moiety)
- GENTIAN VIOLET (UNII: J4Z741D6O5)
- GENTIAN VIOLET (UNII: J4Z741D6O5) (Active Moiety)
Which are Perineze Triple Dye 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:
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Perineze Triple Dye?
- RxCUI: 1188515 - brilliant green 2.29 MG / proflavine 1.14 MG / gentian violet 2.29 MG per 0.61 ML Topical Solution
- RxCUI: 1188515 - brilliant green 3.75 MG/ML / gentian violet 3.75 MG/ML / proflavine 1.87 MG/ML Topical Solution
- RxCUI: 1188520 - Perineze Triple Dye 2.29 MG / 1.14 MG / 2.29 MG per 0.61 ML Topical Solution
- RxCUI: 1188520 - brilliant green 3.75 MG/ML / gentian violet 3.75 MG/ML / proflavine 1.87 MG/ML Topical Solution [Perineze Triple Dye]
- RxCUI: 1188520 - Perineze Triple Dye (brilliant green 3.75 MG/ML / gentian violet 3.75 MG/ML / proflavine 1.87 MG/ML) Topical Solution
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[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".