NDC 73218-002 Flex24 Pain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73218 - Flex24 Inc
- 73218-002 - Flex24 Pain
Product Packages
NDC Code 73218-002-01
Package Description: 7 PATCH in 1 PACKAGE / 1.56 g in 1 PATCH
Product Details
What is NDC 73218-002?
What are the uses for Flex24 Pain?
Which are Flex24 Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Flex24 Pain 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:
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
- BORNEOL (UNII: M89NIB437X)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- CHONDROITIN SULFATE (BOVINE) (UNII: 6IC1M3OG5Z)
- GINGER (UNII: C5529G5JPQ)
- KAEMPFERIA GALANGA ROOT (UNII: 7B7U9D12AI)
- ACONITUM KUSNEZOFFII ROOT (UNII: 3L29I4K8KX)
- LEMON (UNII: 24RS0A988O)
- LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97)
- MINERAL OIL (UNII: T5L8T28FGP)
- MOSCHUS BEREZOVSKII MUSK SAC RESIN (UNII: Z70MFY52S4)
- PETROLATUM (UNII: 4T6H12BN9U)
- ACONITUM NAPELLUS ROOT (UNII: KPD2N7348X)
- ROSIN (UNII: 88S87KL877)
- STAR ANISE (UNII: XKC1657P78)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Flex24 Pain?
- RxCUI: 1364993 - camphor 3 % / menthol 2.52 % Medicated Patch
- RxCUI: 1364993 - camphor 0.03 MG/MG / menthol 0.0252 MG/MG Medicated Patch
- RxCUI: 1494222 - FLEX24 PERFORMANCE 3 % / 2.52 % Medicated Patch
- RxCUI: 1494222 - camphor 0.03 MG/MG / menthol 0.0252 MG/MG Medicated Patch [Flex24 Performance]
- RxCUI: 1494222 - Flex24 Performance (camphor 3 % / menthol 2.52 % ) 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".