NDC 59088-954 Myorx Low Dose Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59088 - Puretek Corporation
- 59088-954 - Myorx
Product Packages
NDC Code 59088-954-05
Package Description: 59 mL in 1 JAR
Product Details
What is NDC 59088-954?
What are the uses for Myorx Low Dose Pain Relieving?
Which are Myorx Low Dose Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Myorx Low Dose Pain Relieving 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BORAGE OIL (UNII: F8XAG1755S)
- CAPSAICIN (UNII: S07O44R1ZM)
- CARBOMER 934 (UNII: Z135WT9208)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- FRUCTOSE (UNII: 6YSS42VSEV)
- HYDROGENATED MENHADEN OIL (UNII: 736VD7888J)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPANEDIOL (UNII: 5965N8W85T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SQUALANE (UNII: GW89575KF9)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- EDETATE SODIUM (UNII: MP1J8420LU)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- TROLAMINE (UNII: 9O3K93S3TK)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
What is the NDC to RxNorm Crosswalk for Myorx Low Dose Pain Relieving?
- RxCUI: 1114454 - menthol 0.5 % Topical Cream
- RxCUI: 1114454 - menthol 5 MG/ML Topical Cream
- RxCUI: 1114456 - Myorx 0.5 % Topical Cream
- RxCUI: 1114456 - menthol 5 MG/ML Topical Cream [Myorx]
- RxCUI: 1114456 - Myorx 5 MG/ML 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".