FDA.reportPublic FDA data

CVS Pain Relief

Product NDC
51316-996
11-digit product format
513160996
Labeler code
51316
Product ID
51316-996_2a8a4561-b693-5cee-e063-6394a90a89e3
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol 10.5%
Dosage form
SPRAY
Route
TOPICAL
Labeler
CVS
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-09-13
Substance
MENTHOL
Active strength
10.5 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
CVS Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL10.5 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui1489073

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-996-04CVS Pain Relief128 g in 1 BOTTLE, SPRAYSPRAY1284
51316-996-10CVS Pain Relief85 g in 1 BOTTLE, SPRAYSPRAY854

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51316-996CVS PAIN RELIEF (MENTHOL 10.5%) SPRAY [CVS]3Current NDC, Legacy NDC, 2 package rows20250101_d0ea80ce-38b2-acde-e053-2995a90a47e5.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1489073menthol 10.5 % Topical SprayPSNd0ea80ce-38b2-acde-e053-2995a90a47e54
1489073menthol 105 MG/ML Topical SpraySCDd0ea80ce-38b2-acde-e053-2995a90a47e54
1489073menthol 10.5 % Topical SpraySYd0ea80ce-38b2-acde-e053-2995a90a47e54

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51316-996-0451316099604128 g in 1 BOTTLE, SPRAY (51316-996-04) 128 g2025-03-31NoNoCurrent
51316-996-105131609961085 g in 1 BOTTLE, SPRAY (51316-996-10) 85 g2022-09-130000-00-00NoNoCurrent