NDC 58228-0103 Prostat Blood Clotting First Aid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58228 - Prostat First Aid
- 58228-0103 - Prostat Blood Clotting First Aid
Product Packages
NDC Code 58228-0103-3
Package Description: 85 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 58228-0103?
What are the uses for Prostat Blood Clotting First Aid?
Which are Prostat Blood Clotting First Aid UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- BENZETHONIUM CHLORIDE (UNII: PH41D05744)
- BENZETHONIUM (UNII: 1VU15B70BP) (Active Moiety)
Which are Prostat Blood Clotting First Aid 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:
- ISOBUTANE (UNII: BXR49TP611)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- KARAYA GUM (UNII: 73W9IQY50Q)
- BUTANE (UNII: 6LV4FOR43R)
- PROPANE (UNII: T75W9911L6)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- TALC (UNII: 7SEV7J4R1U)
- TRAGACANTH (UNII: 2944357O2O)
What is the NDC to RxNorm Crosswalk for Prostat Blood Clotting First Aid?
- RxCUI: 1545716 - benzethonium Cl 0.2 % / lidocaine 4 % Topical Spray
- RxCUI: 1545716 - benzethonium chloride 2 MG/ML / lidocaine 40 MG/ML Topical Spray
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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".