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

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS Pain ReliefMENTHOLCVS Pharmacy4aa629f5-8b8f-cc67-e063-6394a90a019f2026-06-15WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings For external use only Flammable: Keep away from fire or flame and heated surfaces Do not use if you are allergic to any ingredient in this product on open wounds, damaged or irritated skin with a heating pad or TENS device When using this product Use only as directed Avoid contact with eyes or mucous membranes Do not apply to wounds or damaged skin. Do not use wiht other ointments, creams, sprays, or liniments Do not apply to irritated skin or if excessive skin irritation develops Do not bandage Wash hands after use with cool water Do not use with heating pad or device Store in a cool, dry place Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and recur If pregnant or breast feeding, ask a physician before use. Keep out of reach of children and pets. If swallowed, seek professional help and contact Poison Control Center right away.

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