Label: KANGAROO CBD HEATING PAIN RELIEF- methyl salicylate, menthol cream
- NDC Code(s): 72937-118-02, 72937-118-04, 72937-118-08, 72937-118-16
- Packager: SUNSET NOVELTIES, INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 2, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- USES:
- 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.
- IF PREGNANT OR BREAST – FEEDING:
- KEEP OUT OF REACH OF CHILDREN
- STOP USE AND ASK A DOCTOR IF:
- DIRECTIONS:
-
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 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:72937-118-02 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 not final part348 11/29/2022 Labeler - SUNSET NOVELTIES, INC (067218145)