CVS Roll-On

Manufacturer
CVS | Derma Care Research Labs, LLC
Effective date
2024-12-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:43:47

Label at a glance#

ProductCVS Roll-On
Active ingredientCAPSAICIN
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Capsaicin 0.1%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain associated with arthritis, simple backache, sprains, bruises, muscle strains, and cramps.

WARNINGS SECTION

For external use only.

When using this product do not bandage tightly or cover treated area, do not use with heating pad, avoid contact with eyes and mucous membranes, do not apply to wounds, damaged, broken or irritated skin, a transient burning sensation may occur upon application but generally disappears in several days, if severe burning occurs, discontinue use immediately, do not expose the area treated with product to heat or direct sunlight.

Stop use and ask a doctor if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days, redness is present, or irritation develops.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Adults and children of 18 years: apply to affected area, massage into painful area until thoroughly absorbed, repeat as necessary, but no more than 3 to 4 times daily. WASH HANDS WITH SOAP AND WATER AFTER APPLYING. Children 18 years or younger: ask a doctor.

INACTIVE INGREDIENT SECTION

Alcohol denat., aminomethyl propanol, carbomer, glycerin, propylene glycol, water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51316-265-02CVS Roll-On71 g in 1 BOTTLE, PLASTICGEL713

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51316-265CVS ROLL-ON (CAPSAISIN 0.1%) GEL [CVS]3Current NDC, 1 package rows20241217_e8812c49-335e-61ea-e053-2995a90a17aa.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-26551316-265-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CVS Roll-OnCAPSAISIN 0.1%CVSe8812c49-335e-61ea-e053-2995a90a17aa2024-12-15WarningsExact identifier
ndc (package): 51316-265-02
ndc (product): 51316-265
ndc11 (package): 51316026502
spl id: 29574ffa-30bc-85fd-e063-6394a90a74d1
spl set id: e8812c49-335e-61ea-e053-2995a90a17aa

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.