KANGAROO CBD PAIN RELIEVING- menthol gel 
SUNSET NOVELTIES, INC

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72937-040-03

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

Topical Analgesic

USES:

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

For external use only.

Avoid contact with eyes.

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

Ask a health professional before use.

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.

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

KANGAROO PAIN RELIEVING GEL

KANGAROO CBD PAIN RELIEVING 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72937-040
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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
Coloryellow (Light Yellow) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72937-040-0385 g in 1 TUBE; Type 0: Not a Combination Product12/05/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/05/2022
Labeler - SUNSET NOVELTIES, INC (067218145)

Revised: 11/2024
Document Id: 275a6b8d-d4d7-bd8b-e063-6294a90a94e0
Set id: ef15acdb-1733-2b6d-e053-2a95a90ad3d4
Version: 2
Effective Time: 20241120
 
SUNSET NOVELTIES, INC