NDC 58133-055 Berberex Wound Cleanser
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58133-055?
Which are Berberex Wound Cleanser UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Berberex Wound Cleanser 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:
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- ALCOHOL (UNII: 3K9958V90M)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- PANAX QUINQUEFOLIUS WHOLE (UNII: 0P067WOA1X)
What is the NDC to RxNorm Crosswalk for Berberex Wound Cleanser?
- RxCUI: 1437628 - allantoin 0.5 % / benzethonium chloride 0.1 % Topical Solution
- RxCUI: 1437628 - allantoin 5 MG/ML / benzethonium chloride 1 MG/ML Topical Solution
- RxCUI: 1487627 - BerbereX Wound Cleanser 0.5 % / 0.1 % Topical Solution
- RxCUI: 1487627 - allantoin 5 MG/ML / benzethonium chloride 1 MG/ML Topical Solution [Berberex Wound Cleanser]
- RxCUI: 1487627 - Berberex Wound Cleanser (allantoin 0.5 % / benzethonium chloride 0.1 % ) 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".