SanaMax Menthol Pain Relief Cream

Product NDC
72425-210
11-digit product format
724250210
Labeler code
72425
Product ID
72425-210_7e75cf5f-3f35-4e0c-b5c1-23652275a8c1
Type
HUMAN OTC DRUG
Nonproprietary name
MENTHOL
Dosage form
CREAM
Route
TOPICAL
Labeler
SanaMax Plus LLC
Application
part348
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-05-31
Marketing end
0000-00-00
Substance
MENTHOL
Active strength
4 g/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72425-210-03SanaMax Menthol Pain Relief CreamCBD100 mL in 1 TUBECREAM1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72425-210SANAMAX MENTHOL PAIN RELIEF CREAM CBD (MENTHOL) CREAM [SANAMAX PLUS LLC]3Legacy NDC, 1 package rows20250101_21242f22-b2b1-42e1-8b1e-d5e32f49febf.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72425-210-0372425021003100 mL in 1 TUBE (72425-210-03) 100 ml2022-05-310000-00-00NoNoCurrent