NDC 66902-090 Evels Secret Natural Pain Relief Daredevil Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 66902-090-01
Package Description: 29.57 mL in 1 CONTAINER
NDC Code 66902-090-02
Package Description: 59.15 mL in 1 CONTAINER
NDC Code 66902-090-03
Package Description: 88.72 mL in 1 CONTAINER
NDC Code 66902-090-04
Package Description: 118.29 mL in 1 CONTAINER
NDC Code 66902-090-05
Package Description: 14.79 mL in 1 CONTAINER
NDC Code 66902-090-08
Package Description: 236.59 mL in 1 CONTAINER
NDC Code 66902-090-16
Package Description: 473.18 mL in 1 CONTAINER
NDC Code 66902-090-28
Package Description: 3785.41 mL in 1 CONTAINER
Product Details
What is NDC 66902-090?
What are the uses for Evels Secret Natural Pain Relief Daredevil Strength?
Which are Evels Secret Natural Pain Relief Daredevil Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Evels Secret Natural Pain Relief Daredevil Strength 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:
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Evels Secret Natural Pain Relief Daredevil Strength?
- RxCUI: 259249 - menthol 10 % Topical Gel
- RxCUI: 259249 - menthol 0.1 MG/MG 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".