KANGAROO CBD PAIN RELIEF

Manufacturer
SUNSET NOVELTIES, INC
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:49:03

Label at a glance#

ProductKANGAROO CBD PAIN RELIEF
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure12 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.

Dosage and administration

Adults and children over 12 years of age; apply a thin layer to affected area and scrub gently not more than 3 to 4 times a day. Wash hands with soap and water after use. Children under 12 years of age; do not use unless directed by doctor/physician

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Camphor 3%

OTC - PURPOSE SECTION

External Analgesic

Pain Relieving

USES:

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.

WARNINGS SECTION

Use only as directed. For external use only. Do not bandage tightly. Do not use with heating pad, pack, wrap, hot water bottle or any heating element. Keep away from children. package is not child resistant. In case of accidental ingestion, contact doctor immediately. If prone to allergic reaction to the product, consult to a doctor before using.

OTC - WHEN USING SECTION

Avoid contact with eyes, mucous membranes, rashes, wounds or damaged skin.
Do not apply on nose and genital area.

If rash, redness or itchiness results; discontinue use and consult a doctor.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years of age; apply a thin layer to affected area and scrub gently not more than 3 to 4 times a day.
Wash hands with soap and water after use.

Children under 12 years of age; do not use unless directed by doctor/physician

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children. Package not child resistant.

INACTIVE INGREDIENT SECTION

Aqua, Paraffinum Liquidum, Alcohol Denat, Stearic Acid, Cetearyl Alcohol, Polysorbate 60, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Glycereth-26, Propylene Glycol, Diazolidinyl Urea, Methylparaben, Propylparaben, Tocopheryl Acetate, Cannabis Sativa Seed Oil, Stearyl Alcohol, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Polysorbate 20, Triethanolamine, Parfum, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Sodium Benzotriazolyl Butylphenol Sulfonate, Buteth-3, Tributyl Citrate, Cannabidiol, FD&C Blue #1 Powder (CI 42090), Linalool, Limonene, Benzyl Benzoate, Coumarin, Geraniol.

KANGAROO CBD PAIN RELIEF CREAM 2oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO CBD PAIN RELIEF CREAM 2KANGAROO CBD PAIN RELIEF CREAM 2

KANGAROO CBD PAIN RELIEF CREAM 4oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO CBD PAIN RELIEF CREAM 4KANGAROO CBD PAIN RELIEF CREAM 4

KANGAROO CBD PAIN RELIEF CREAM 8oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO CBD PAIN RELIEF CREAM 8KANGAROO CBD PAIN RELIEF CREAM 8

KANGAROO CBD PAIN RELIEF CREAM 16 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO PAIN RELIEF 16KANGAROO PAIN RELIEF 16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72937-301KANGAROO CBD PAIN RELIEF (MENTHOL, CAMPHOR) CREAM [SUNSET NOVELTIES, INC]3Legacy NDC20241122_eec87c70-b340-405c-e053-2995a90a1050.zip

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72937-30172937-301-02, 72937-301-04, 72937-301-08, 72937-301-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 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
44141d2a-1d92-b970-e063-6294a90a53f4eec87c70-b340-405c-e053-2995a90a10502025-11-20WarningsExact identifier
spl set id: eec87c70-b340-405c-e053-2995a90a1050

Reported adverse events (FAERS/openFDA)#

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