KANGAROO CBD PAIN RELIEVING- menthol gel

KANGAROO CBD PAIN RELIEVING by

Drug Labeling and Warnings

KANGAROO CBD PAIN RELIEVING by is a Otc medication manufactured, distributed, or labeled by SUNSET NOVELTIES, INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

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

PURPOSE

Topical Analgesic

USES:

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

WARNINGS

For external use only.

Avoid contact with eyes.

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

PREGNANCY OR BREAST FEEDING

Ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS:

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

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

INGREDIENTS AND APPEARANCE

KANGAROO CBD PAIN RELIEVING 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72937-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBIC ACID (UNII: X045WJ989B)
METHYL SALICYLATE (UNII: LAV5U5022Y)
CANNABIDIOL (UNII: 19GBJ60SN5)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SALICYLIC ACID (UNII: O414PZ4LPZ)
CARBOMER 940 (UNII: 4Q93RCW27E)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
BENZYL ALCOHOL (UNII: LKG8494WBH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALCOHOL (UNII: 3K9958V90M)
CETEARETH-25 (UNII: 8FA93U5T67)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
TEA TREE OIL (UNII: VIF565UC2G)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Characteristics
Color	yellow (Light Yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72937-040-03	85 g in 1 TUBE; Type 0: Not a Combination Product	12/05/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/05/2022

Labeler - SUNSET NOVELTIES, INC (067218145)