NDC 51395-412 Top Safety First Aid Burn Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51395-412?
What are the uses for Top Safety First Aid Burn Cream?
Which are Top Safety First Aid Burn Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Top Safety First Aid Burn Cream 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:
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- METHYLCELLULOSE (25 MPA.S) (UNII: BI55GG2WLI)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETETH-20 (UNII: I835H2IHHX)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
- PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Top Safety First Aid Burn Cream?
- RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
- RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
- RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
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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".