KANGAROO CBD PAIN RELIEF- menthol, camphor cream

KANGAROO CBD PAIN RELIEF by

Drug Labeling and Warnings

KANGAROO CBD 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

Menthol 10%

Camphor 3%

PURPOSE

External Analgesic

Pain Relieving

USES:

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

WARNINGS

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.

WHEN USING

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:

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

KEEP OUT OF REACH OF CHILDREN

Keep away from children. Package not child resistant.

INACTIVE INGREDIENT

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

KANGAROO CBD PAIN RELIEF CREAM 4oz

KANGAROO CBD PAIN RELIEF CREAM 8oz

KANGAROO CBD PAIN RELIEF CREAM 16 oz

INGREDIENTS AND APPEARANCE

KANGAROO CBD PAIN RELIEF 
menthol, camphor cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72937-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g  in 100 g
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TRIBUTYL CITRATE (UNII: 827D5B1B6S)
PANTHENOL (UNII: WV9CM0O67Z)
HYDROXYPROLINE (UNII: RMB44WO89X)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) (UNII: M4PPW69Y4H)
GLYCERETH-26 (UNII: NNE56F2N14)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
BUTETH-3 (UNII: OC116GRO69)
BASIC BLUE 1 (UNII: 92N74OA24D)
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
METHYLPARABEN (UNII: A2I8C7HI9T)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
TRIDECETH-6 (UNII: 3T5PCR2H0C)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)
POLYSORBATE 60 (UNII: CAL22UVI4M)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE 1000 (UNII: MCU2324216)
TROLAMINE (UNII: 9O3K93S3TK)
ACETYLTRIBUTYL CITRATE (UNII: 0ZBX0N59RZ)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
ALCOHOL (UNII: 3K9958V90M)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
MINERAL OIL (UNII: T5L8T28FGP)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CANNABIDIOL (UNII: 19GBJ60SN5)

Product Characteristics
Color	green	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72937-301-02	56 g in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2022
2	NDC: 72937-301-04	112 g in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2022
3	NDC: 72937-301-08	224 g in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2022
4	NDC: 72937-301-16	448 g in 1 BOTTLE; Type 0: Not a Combination Product	12/14/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/01/2022

Labeler - SUNSET NOVELTIES, INC (067218145)