NDC 50730-1450 Alcohol Prep Swab With Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50730 - H And P Industries, Inc. Dba Triad Group
- 50730-1450 - Alcohol Prep Swab With Pain Relief
Product Packages
NDC Code 50730-1450-1
Package Description: 100 PACKET in 1 CARTON / 1 SWAB in 1 PACKET
Product Details
What is NDC 50730-1450?
What are the uses for Alcohol Prep Swab With Pain Relief?
Which are Alcohol Prep Swab With Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
Which are Alcohol Prep Swab With Pain Relief 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Alcohol Prep Swab With Pain Relief?
- RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Medicated Pad
- RxCUI: 809206 - benzocaine 60 MG/ML / isopropyl alcohol 0.7 ML/ML Medicated Pad
- RxCUI: 809206 - benzocaine 6 % / isopropyl alcohol 70 % Topical Swab
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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".