NDC 73279-0005 Toplast Pain Relief Lidocaine 4percent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73279 - Icure Pharmaceutical Inc, Wanju Factory
- 73279-0005 - Toplast Pain Relief Lidocaine 4percent
Product Packages
NDC Code 73279-0005-2
Package Description: 5 POUCH in 1 CARTON / 1 PATCH in 1 POUCH (73279-0005-1)
Product Details
What is NDC 73279-0005?
What are the uses for Toplast Pain Relief Lidocaine 4percent?
Which are Toplast Pain Relief Lidocaine 4percent UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Toplast Pain Relief Lidocaine 4percent 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- UREA (UNII: 8W8T17847W)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
- GELATIN (UNII: 2G86QN327L)
- KAOLIN (UNII: 24H4NWX5CO)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TARTARIC ACID (UNII: W4888I119H)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Toplast Pain Relief Lidocaine 4percent?
- RxCUI: 1737778 - lidocaine 4 % Medicated Patch
- RxCUI: 1737778 - lidocaine 0.04 MG/MG Medicated Patch
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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".