NDC 70897-001 First Aid Burn Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70897 - Davemed Healthcare Co., Ltd
- 70897-001 - First Aid Burn Cream
Product Packages
NDC Code 70897-001-01
Package Description: .9 g in 1 BAG
NDC Code 70897-001-02
Package Description: 42.5 g in 1 BAG
Product Details
What is NDC 70897-001?
What are the uses for First Aid Burn Cream?
Which are 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 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- MINERAL OIL (UNII: T5L8T28FGP)
- METHYL PARAOXON (UNII: UE1A2XL95H)
- PETROLATUM (UNII: 4T6H12BN9U)
- DIISOPROPYL PARAOXON (UNII: R90A2849YV)
- ALLANTOIN (UNII: 344S277G0Z)
- TRIETHANOLAMINE SULFATE (UNII: MV1V89M17O)
- STEARIC ACID D7 (UNII: T3B081197X)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
What is the NDC to RxNorm Crosswalk for 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".