NDC 65373-401 Ortho-nesic With Capsaicin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65373 - Blaine Labs Inc.
- 65373-401 - Ortho-nesic With Capsaicin
Product Packages
NDC Code 65373-401-01
Package Description: 170 g in 1 TUBE
NDC Code 65373-401-02
Package Description: 907 g in 1 BOTTLE, PUMP
NDC Code 65373-401-03
Package Description: 3629 g in 1 BOTTLE, PUMP
NDC Code 65373-401-04
Package Description: 85 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 65373-401?
What are the uses for Ortho-nesic With Capsaicin?
Which are Ortho-nesic With Capsaicin UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Ortho-nesic With Capsaicin 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)
- ALCOHOL (UNII: 3K9958V90M)
- CARBOMER 934 (UNII: Z135WT9208)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- TROLAMINE (UNII: 9O3K93S3TK)
- CAPSAICIN (UNII: S07O44R1ZM)
What is the NDC to RxNorm Crosswalk for Ortho-nesic With Capsaicin?
- RxCUI: 1087242 - Ortho-Nesic 0.2 % / 3.5 % Topical Gel
- RxCUI: 1087242 - camphor 0.002 MG/MG / menthol 0.035 MG/MG Topical Gel [Ortho-Nesic]
- RxCUI: 1087242 - Ortho-Nesic (camphor 0.002 MG/MG / menthol 0.035 MG/MG) Topical Gel
- RxCUI: 1087242 - Ortho-Nesic (camphor 0.2 % / menthol 3.5 % ) Topical Gel
- RxCUI: 416207 - camphor 0.2 % / menthol 3.5 % 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".