Label: MY HEMP MD CBD MUSCLE AND JOINT CREAM- menthol and methyl salicylate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 52261-5201-0, 52261-5201-2, 52261-5201-3 - Packager: Cosco International, 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 November 1, 2019
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- Warnings:
- Directions:
- Other information:
- Inactive ingredients:
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MY HEMP MD CBD MUSCLE AND JOINT CREAM
menthol and methyl salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52261-5201 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.05 in 1 kg METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.10 kg in 1 kg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARBOMER COPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 1N11AG4X4L) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) DIMETHYL SULFOXIDE (UNII: YOW8V9698H) N-ACETYLGLUCOSAMINE (UNII: V956696549) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) POLYSORBATE 80 (UNII: 6OZP39ZG8H) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) HEMP (UNII: TD1MUT01Q7) CANNABIDIOL (UNII: 19GBJ60SN5) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52261-5201-2 1 in 1 CARTON 11/01/2019 1 NDC:52261-5201-0 0.088 kg in 1 TUBE; Type 0: Not a Combination Product 2 NDC:52261-5201-3 0.001 kg in 1 PACKET; Type 0: Not a Combination Product 11/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/01/2019 Labeler - Cosco International, Inc. (016433141) Registrant - Cosco International, Inc. (016433141) Establishment Name Address ID/FEI Business Operations Cosco International, Inc. 016433141 manufacture(52261-5201) , label(52261-5201) , pack(52261-5201)