KANGAROO CBD HEATING PAIN RELIEF

Manufacturer
SUNSET NOVELTIES, INC
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:40:34

Label at a glance#

ProductKANGAROO CBD HEATING PAIN RELIEF
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure12 sections

Dosage and administration

Adults and Children over 12 years • Apply a small amount on the affected area.• Massage in circular motion, let set for a few seconds.• Repeat as necessary, but no more than 3 to 4 times daily. • Wash hands with soap and water after use. Children under 12 years of age consult a doctor

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 18%

Menthol 10%

OTC - PURPOSE SECTION

Topical Analgesic.

USE

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

• For external use only. • Ask a doctor before use if you have
redness over affected area.

OTC - WHEN USING SECTION

Use only as directed
Do not bandage tightly or use with a heating pad
Avoid contact with eyes and mucous membranes
Do not apply to wounds or damaged, broken or irritated skin

A transient burning sensation or redness may occur upon application but generally disappears in several days.
If you experience an allergic reaction, discontinue use and consult a doctor.

Do not expose the area treated with product to heat or direct sunlight.

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

Condition worsens
Redness is present
Irritation develops
Symptoms persist for more than 7 days or clear up occur again within a few days

You experience signs injury, such as pain, swelling or blistering where the product was applied.

IF PREGNANT OR BREAST – FEEDING

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 12 years • Apply a small amount on
the affected area.• Massage in circular motion, let set for a few seconds.•
Repeat as necessary, but no more than 3 to 4 times daily. • Wash hands with
soap and water after use. Children under 12 years of age consult a doctor

OTHER SAFETY INFORMATION

Store tightly closed in a dry place at controlled room
temperature between 59°-86° F (15°-30° C).

INACTIVE INGREDIENT SECTION

Water (Aqua), Paraffinum Liquidum, Glyceryl Stearate, Stearic Acid, Cetyl Alcohol, Dimethicone, Glycereth-26, Acrylamide/Sodium
Acrylate Copolymer, Trideceth-6, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol, Stearyl Alcohol, Triethanolamine, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Cannabidiol, FD&C Yellow No.6 (CI 15985).

KANGAROO CBD HEATING PAIN RELIEF CREAM SACHET

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

kangaroo heating cream sachetkangaroo heating cream sachet

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codedrive.google.com/drive/folders/1ktHScL9OFt17X1lAlBmCHML9ec945bLG?usp=sharingkangaroo heating pain relief sachet 72937-118-33.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
4d7a96d5-8256-4268-9a6c-25ea66d321feProduct name120180814

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72937-11872937-118-33

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
4414470b-2a21-82e2-e063-6394a90a756612893bcb-6db2-76d7-e063-6294a90ac3232025-11-20WarningsExact identifier
spl id: 4414470b-2a21-82e2-e063-6394a90a7566
spl set id: 12893bcb-6db2-76d7-e063-6294a90ac323

Reported adverse events (FAERS/openFDA)#

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