Label: KANGAROO CBD HEATING PAIN RELIEF- methyl salicylate, menthol cream
- NDC Code(s): 72937-118-33
- Packager: SUNSET NOVELTIES, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 29, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USE
- WARNINGS
-
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 skinA 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.
- STOP USE AND ASK A DOCTOR IF
- IF PREGNANT OR BREAST – FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
Water (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 No.6 (CI 15985). - KANGAROO CBD HEATING PAIN RELIEF CREAM SACHET
-
INGREDIENTS AND APPEARANCE
KANGAROO CBD HEATING PAIN RELIEF
methyl salicylate, menthol creamProduct 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:72937-118-33 10 mL in 1 PACKET; Type 0: Not a Combination Product 03/10/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 03/10/2024 Labeler - SUNSET NOVELTIES, INC (067218145)