NDC 52124-0114 Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52124 - Genuine First Aid Llc
- 52124-0114 - Protection
Product Characteristics
Product Packages
NDC Code 52124-0114-1
Package Description: 1 KIT in 1 KIT
Product Details
What is NDC 52124-0114?
What are the uses for Protection?
Which are Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Protection 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)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- SACCHARIN (UNII: FST467XS7D)
- SODIUM CATION (UNII: LYR4M0NH37)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Protection?
- RxCUI: 1046313 - benzocaine 6 % / ethanol 60 % Medicated Pad
- RxCUI: 1046313 - benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad
- RxCUI: 1046313 - benzocaine 6 % / ethanol 60 % Topical Swab
- RxCUI: 318272 - aspirin 81 MG Chewable Tablet
- RxCUI: 318272 - ASA 81 MG Chewable Tablet
* Please review the disclaimer below.
[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".