NDC 54723-667 Eclipse Topical Anesthetic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54723 - Sambria Pharmaceuticals
- 54723-667 - Eclipse Topical Anesthetic
Product Packages
NDC Code 54723-667-04
Package Description: 4 g in 1 PACKET
NDC Code 54723-667-05
Package Description: .005 g in 1 PACKET
NDC Code 54723-667-10
Package Description: 2 g in 1 PACKET
Product Details
What is NDC 54723-667?
What are the uses for Eclipse Topical Anesthetic?
Which are Eclipse Topical Anesthetic UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Eclipse Topical Anesthetic 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)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)
- EMU OIL (UNII: 344821WD61)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- LAURETH-7 (UNII: Z95S6G8201)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Eclipse Topical Anesthetic?
- RxCUI: 1010895 - lidocaine HCl 4 % Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 40 MG/ML Topical Cream
- RxCUI: 1010895 - lidocaine hydrochloride 4 % Topical Cream
* 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".