FDA.reportPublic FDA data

KANGAROO CBD PAIN RELIEVING

Manufacturer
SUNSET NOVELTIES, INC
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:49:03

Label at a glance#

ProductKANGAROO CBD PAIN RELIEVING
Active ingredientMENTHOL
Label structure9 sections

Indications and uses

Aid for temporary local relief of minor pain in muscles or joints.

Dosage and administration

Adults and Children over two years: Apply to affected area no more than three to four times daily. Children under two-years of age: Consult a physician.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol ………………………………...…………………………….…. 4%

OTC - PURPOSE SECTION

Topical Analgesic

USES:

INDICATIONS & USAGE SECTION

Aid for temporary local relief of minor pain in muscles or joints.

WARNINGS SECTION

For external use only.

Avoid contact with eyes.

If symptoms persist for more than seven days, discontinue use and consult physician.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and Children over two years:

Apply to affected area no more than three to four times daily.

Children under two-years of age: Consult a physician.

INACTIVE INGREDIENT SECTION

Aqua, Alcohol Denat, Ceteareth-25, Glycerin, Benzyl Alcohol, Salicylic Acid, Sorbic Acid, Caprylic/Capric Triglyceride, Parfum, Aloe Barbadensis Leaf Extract, Carbomer, Sodium Hydroxide, Cannabidiol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methyl Salicylate, FD&C Yellow 5 (CI 19140), Geraniol, Hexyl Cinnamal, Amyl cinnamal, Citronellol, Hydroxycitronellal, Linalool, Coumarin.

KANGAROO PAIN RELIEVING GEL 3oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO PAIN RELIEVING GELKANGAROO PAIN RELIEVING GEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72937-040KANGAROO CBD PAIN RELIEVING (MENTHOL) GEL [SUNSET NOVELTIES, INC]2Legacy NDC20241122_ef15acdb-1733-2b6d-e053-2a95a90ad3d4.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72937-04072937-040-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
SORBIC ACIDX045WJ989BIACT
METHYL SALICYLATELAV5U5022YIACT
CANNABIDIOL19GBJ60SN5IACT
MENTHOLL7T10EIP3AACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SALICYLIC ACIDO414PZ4LPZIACT
CARBOMER 9404Q93RCW27EIACT
SODIUM HYDROXIDE55X04QC32IIACT
BENZYL ALCOHOLLKG8494WBHIACT
ALOE VERA LEAFZY81Z83H0XIACT
ALCOHOL3K9958V90MIACT
CETEARETH-258FA93U5T67IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
TEA TREE OILVIF565UC2GIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
4424d5bf-28bb-56c8-e063-6294a90a8dafef15acdb-1733-2b6d-e053-2a95a90ad3d42025-11-21WarningsExact identifier
spl set id: ef15acdb-1733-2b6d-e053-2a95a90ad3d4

Reported adverse events (FAERS/openFDA)#

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