ActivICE

Product NDC
53329-996
11-digit product format
533290996
Labeler code
53329
Product ID
53329-996_41d71f1f-b6a8-5401-e063-6294a90a19d3
Type
HUMAN OTC DRUG
Nonproprietary name
menthol
Dosage form
SPRAY
Route
TOPICAL
Labeler
Medline Industries, LP
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-01-01
Substance
MENTHOL
Active strength
100 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ActivICE
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL100 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui667889

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53329-996-04ActivICE118 mL in 1 BOTTLESPRAY1186

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53329-996ACTIVICE (MENTHOL) SPRAY [MEDLINE INDUSTRIES, LP]5Current NDC, Legacy NDC, 1 package rows20241215_98fa9a34-0e1e-0997-e053-2a95a90ac77d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
667889menthol 10 % Topical SprayPSN98fa9a34-0e1e-0997-e053-2a95a90ac77d6
667889menthol 100 MG/ML Topical SpraySCD98fa9a34-0e1e-0997-e053-2a95a90ac77d6
667889menthol 10 % Topical SpraySY98fa9a34-0e1e-0997-e053-2a95a90ac77d6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53329-996-0453329099604118 mL in 1 BOTTLE (53329-996-04) 118 ml2020-01-010000-00-00NoNoCurrent