CVS Pain Relief

Product NDC
51316-997
11-digit product format
513160997
Labeler code
51316
Product ID
51316-997_28f15d7e-f9cc-4807-e063-6294a90ab6f7
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol 4%
Dosage form
GEL
Route
TOPICAL
Labeler
CVS
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-09-29
Substance
MENTHOL
Active strength
4 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
MENTHOL4 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui415974

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-997-04CVS Pain Relief85 g in 1 TUBEGEL853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51316-997CVS PAIN RELIEF (MENTHOL 4%) GEL [CVS]3Current NDC, Legacy NDC, 1 package rows20241213_d1660d55-1ee0-7aa2-e053-2995a90a6579.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSNd1660d55-1ee0-7aa2-e053-2995a90a65793
415974menthol 0.04 MG/MG Topical GelSCDd1660d55-1ee0-7aa2-e053-2995a90a65793
415974menthol 4 % Topical GelSYd1660d55-1ee0-7aa2-e053-2995a90a65793

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
51316-997-045131609970485 g in 1 TUBE (51316-997-04) 85 g2020-09-290000-00-00NoNoCurrent