KANGAROO CBD COOLING PAIN RELIEF

Manufacturer
SUNSET NOVELTIES, INC
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:49:03

Label at a glance#

ProductKANGAROO CBD COOLING PAIN RELIEF
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure13 sections

Indications and uses

Aid for temporary local relief of minor aches of muscles and joints associated with simple backache, arthritis, sprains, and strains

Dosage and administration

Adults and Children over 12 years: Apply a small amount on desired area. Massage in circular motions until absorbed Repeat as necessary, but no more than 3 to 4 times per day. Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C). Wash hands with soap and water after use.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 6%

Camphor 2%

OTC - PURPOSE SECTION

Topical Analgesic.

Pain Relieving.

USES:

INDICATIONS & USAGE SECTION

Aid for temporary local relief of minor aches 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 or use with a heating pad, pack, wrap, hot water bottle or any heating element. Keep away from children, Package 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 and mucous membranes, rashes wounds or damaged skin
Do not apply to wounds or damaged, broken or irritated skin

Do not apply on nose and genital area.
If rash, redness or itchiness results; discontinue use and consult a doctor.

If pregnant or breast-feeding ask a health professional before use.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years:

Apply a small amount on desired area.
Massage in circular motions until absorbed
Repeat as necessary, but no more than 3 to 4 times per day.
Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

Wash hands with soap and water after use.

STOP USE AND ASK A DOCTOR IF:

OTC - STOP USE SECTION

Conditions worsen
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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INACTIVE INGREDIENT SECTION

Aqua, Alcohol Denat, Propylene Glycol, Salicylic Acid, Glycerin, Polysorbate 20, Carbomer, Sodium Hydroxide, Mentha Arvensis Herb Oil, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Cannabis Sativa Seed Oil, Benzyl Alcohol, Sorbic Acid, Cannabidiol, FD&C Blue. 1 Powder (CI 42090), FD&C Yellow. 5 (CI 19140).

KANGAROO CBD COOLING PAIN RELIEF GEL 2 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO COOLING PAIN RELIEF 2KANGAROO COOLING PAIN RELIEF 2

KANGAROO CBD COOLING PAIN RELIEF GEL 4 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO COOLING PAIN RELIEF 4KANGAROO COOLING PAIN RELIEF 4

KANGAROO CBD COOLING PAIN RELIEF GEL 8 oz

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO COOLING PAIN RELIEF 8KANGAROO COOLING PAIN RELIEF 8

KANGAROO CBD COOLING PAIN RELIEF GEL 16 OZ

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KANGAROO COOLING PAIN RELIEF 16KANGAROO COOLING PAIN RELIEF 16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72937-062KANGAROO CBD COOLING PAIN RELIEF (MENTHOL, CAMPHOR) GEL [SUNSET NOVELTIES, INC]4Legacy NDC20241122_eea1093b-2876-5c58-e053-2995a90aca20.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72937-06272937-062-02, 72937-062-04, 72937-062-08, 72937-062-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
44143742-7797-ca7b-e063-6294a90a21b8eea1093b-2876-5c58-e053-2995a90aca202025-11-20WarningsExact identifier
spl set id: eea1093b-2876-5c58-e053-2995a90aca20

Reported adverse events (FAERS/openFDA)#

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