KANGAROO CBD HEATING PAIN RELIEF- methyl salicylate, menthol cream

KANGAROO CBD HEATING PAIN RELIEF by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Methyl Salicylate 18%

Menthol 10%

PURPOSE

Topical Analgesic.

USES:

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

WARNINGS

For external use only.

WHEN USING

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.

IF PREGNANT 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.

STOP USE AND ASK A DOCTOR IF:

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.

DIRECTIONS:

Adults an childre over 12 years of age: apply a thin layer to affected areaand rub gently no more than 3 to 4 times daily.

Wash hands with soap and water after use.

children undre 12 years of age; do not use unless directed by a doctor/physician.

Store at room temperature 15°C - 30°C.

INACTIVE INGREDIENT

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 #6 (CI 15985).

KANGAROO CBD HEATING PAIN RELIEF CREAM 2 oz

KANGAROO CBD HEATING PAIN RELIEF CREAM 4 oz

KANGAROO CBD HEATING PAIN RELIEF CREAM 8 oz

KANGAROO CBD HEATING PAIN RELIEF CREAM 16 oz

INGREDIENTS AND APPEARANCE

KANGAROO CBD HEATING PAIN RELIEF 
methyl salicylate, menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72937-118
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	9.8 g  in 100 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	17.6 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERETH-26 (UNII: NNE56F2N14)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
COMFREY LEAF (UNII: DG4F8T839X)
CANNABIDIOL (UNII: 19GBJ60SN5)
AMINO ACIDS, WHEAT (UNII: 0370GZL32F)
WATER (UNII: 059QF0KO0R)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
PANTHENOL (UNII: WV9CM0O67Z)
HYDROXYPROLINE (UNII: RMB44WO89X)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIMETHICONE 1000 (UNII: MCU2324216)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
TROLAMINE (UNII: 9O3K93S3TK)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
MINERAL OIL (UNII: T5L8T28FGP)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Product Characteristics
Color	orange (Light Orange)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72937-118-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/29/2022
2	NDC: 72937-118-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/29/2022
3	NDC: 72937-118-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/29/2022
4	NDC: 72937-118-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/29/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	11/29/2022

Labeler - SUNSET NOVELTIES, INC (067218145)