NDC 55301-044 Exchange Select Burn Relief Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55301 - Army And Air Force Exchange Service
- 55301-044 - Exchange Select Burn Relief
Product Packages
NDC Code 55301-044-16
Package Description: 227 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 55301-044?
What are the uses for Exchange Select Burn Relief Pain Relieving?
Which are Exchange Select Burn Relief Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Exchange Select Burn Relief Pain Relieving 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)
- TROLAMINE (UNII: 9O3K93S3TK)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- MENTHOL (UNII: L7T10EIP3A)
What is the NDC to RxNorm Crosswalk for Exchange Select Burn Relief Pain Relieving?
- RxCUI: 1011849 - lidocaine HCl 0.5 % Topical Gel
- RxCUI: 1011849 - lidocaine hydrochloride 0.005 MG/MG Topical Gel
- RxCUI: 1011849 - lidocaine hydrochloride 0.5 % Topical Gel
* 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".