CVS Pain Relief

Product NDC
51316-933
11-digit product format
513160933
Labeler code
51316
Product ID
51316-933_4aa629f5-8b90-cc67-e063-6394a90a019f
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
GEL
Route
TOPICAL
Labeler
CVS Pharmacy
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-02-12
Substance
MENTHOL, UNSPECIFIED FORM
Active strength
40 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
CVS Pain Relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL, UNSPECIFIED FORM40 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui415974

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
51316-933-03CVS Pain Relief89 mL in 1 TUBEGEL891
51316-933-25CVS Pain Relief74 mL in 1 BOTTLEGEL741

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
415974menthol 4 % Topical GelPSN4aa629f5-8b8f-cc67-e063-6394a90a019f1
415974menthol 0.04 MG/MG Topical GelSCD4aa629f5-8b8f-cc67-e063-6394a90a019f1
415974menthol 4 % Topical GelSY4aa629f5-8b8f-cc67-e063-6394a90a019f1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
51316-933-035131609330389 mL in 1 TUBE (51316-933-03) 89 ml2026-02-12NoNoCurrent
51316-933-255131609332574 mL in 1 BOTTLE (51316-933-25) 74 ml2026-02-12NoNoCurrent