NDC 69329-002 Lidonexe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69329 - Patchwerx Labs, Inc.
- 69329-002 - Lidonexe
Product Packages
NDC Code 69329-002-05
Package Description: 5 PATCH in 1 BOX / 10 g in 1 PATCH
NDC Code 69329-002-25
Package Description: 25 PATCH in 1 BOX / 10 g in 1 PATCH
Product Details
What is NDC 69329-002?
What are the uses for Lidonexe?
Which are Lidonexe UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Lidonexe 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:
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TROLAMINE (UNII: 9O3K93S3TK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Lidonexe?
- RxCUI: 1373130 - lidocaine HCl 4 % / menthol 1 % Medicated Patch
- RxCUI: 1373130 - lidocaine hydrochloride 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch
* 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".