Target Up and Up Pain Relief Menthol Topical Analgesic

Product NDC
82442-430
11-digit product format
824420430
Labeler code
82442
Product ID
82442-430_4910f32f-c63a-0215-e063-6394a90a1c7b
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
SPRAY
Route
TOPICAL
Labeler
Target Corporation
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-04-01
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
10.5 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Target Up and Up Pain Relief Menthol Topical Analgesic
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM10.5 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui1489073

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
82442-430-03Target Up and Up Pain Relief Menthol Topical Analgesic85 g in 1 CANSPRAY851

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1489073menthol 10.5 % Topical SprayPSN4910f32f-c639-0215-e063-6394a90a1c7b1
1489073menthol 105 MG/ML Topical SpraySCD4910f32f-c639-0215-e063-6394a90a1c7b1
1489073menthol 10.5 % Topical SpraySY4910f32f-c639-0215-e063-6394a90a1c7b1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82442-430-038244204300385 g in 1 CAN (82442-430-03) 85 g2026-04-01NoNoHistorical