Evel Knievels Natural Choice Pain Relief

Product NDC
66902-195
11-digit product format
669020195
Labeler code
66902
Product ID
66902-195_2501c6e2-294b-3ec6-e063-6394a90ad9e7
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol, unspecified form
Dosage form
GEL
Route
TOPICAL
Labeler
Natural Essentials, Inc.
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-05-29
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
100 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Evel Knievels Natural Choice Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM100 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66902-195-03Evel Knievels Natural Choice Pain Relief85 g in 1 BOTTLEGEL856

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66902-195EVEL KNIEVELS NATURAL CHOICE PAIN RELIEF (MENTHOL, UNSPECIFIED FORM) GEL [NATURAL ESSENTIALS, INC.]6Current NDC, Legacy NDC, 1 package rows20241024_4576656c-4b6e-6965-7665-6c52756c6573.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66902-195-036690201950385 g in 1 BOTTLE (66902-195-03) 85 g2020-05-290000-00-00NoNoCurrent