Label: HEMPVANA MAXIMUM STRENGTH PAIN RELIEF - PLATINUM- trolamine salicylate cream

  • NDC Code(s): 73287-021-01, 73287-021-02
  • Packager: TELEBRANDS CORP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 22, 2024

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  • Active ingredient

    Trolamine Salicylate 10%

  • Purpose

    Trolamine Salicylate 10%..........Topical Analgesic

  • Uses

    temporarily relieves minor pain associated with:

    • arthritis
    • simple backache
    • muscle strains
    • sprains
    • bruises
  • Warnings

    For external use only

    Allergy alert:If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

    When using this product

    • Use only as directed. Read and follow all directions and warnings on this label.
    • Do not bandage tightly or apply local heat (such as heating pads) to the area of use.
    • Avoid contact with eyes or mucous membranes.
    • Do not apply to wounds or damaged, broken or irritated skin.
    • Do not use at the same time as other topical analgesics.

    Stop use and ask a doctor if

    • Condition worsens
    • Symptoms persist for more than 7 days or clear up and occur again within a few days
    • Redness is present or irritation develops

    If pregnant or breast-feeding,ask a health professional before use.

    Keep out of reach of children and pets.If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Adults and children 2 years of age and older:Apply to affected area not more than 3 to 4 times daily
    • Children under 2 years of age:Consult a physician
    • Massage into painful area until thoroughly absorbed into skin.
    • REpeat as necessary, but no more than 4 times daily.
  • Inactive ingredients

    Water/Aqua/Eau, Ethylhexyl Stearate, Cannabis Sativa (Hemp) Seed Oil, Butylene Glycol, Stearic Acid, DImethicone, Caprylic/Capric Trigylceride, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Glycerin, Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Curcuma Longa (Turmeric) Root Extract, Dimethyl Sulfone, Tocopheryl Acetate, Phenoxyethanol, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Isohexadecane, Ethylhexylglycerin, Hexylene Glycol, Allantoin, Mannitol, Microcrystalline Cellulose, Iron Oxides Yellow (CI 77492), Tocopherol, Hydroxypropyl Methylcellulose, Ubiquinone, Polysorbate 80, Sodium Hydroxide, Disodium EDTA, Yellow 6 (CI 15985), Blue 1 (CI 42090)

  • Questions?

    Call (855) 877-4503 (M-F, 9am-5pm EST)

  • PRINCIPAL DISPLAY PANEL

    Hempvana

    Maximum Strength Pain Relief Cream

    Platinum

    +4x Hemp* Seed Oil

    For Moisturization

    Trolamine Salicylate 10%

    For Pain

    Net Wt. 4 oz (119 g)

    *Compared to original Hempvana Pain Relief Cream

    1

  • INGREDIENTS AND APPEARANCE
    HEMPVANA MAXIMUM STRENGTH PAIN RELIEF - PLATINUM 
    trolamine salicylate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73287-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ) TROLAMINE SALICYLATE10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    TURMERIC (UNII: 856YO1Z64F)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    UBIDECARENONE (UNII: EJ27X76M46)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    MANNITOL (UNII: 3OWL53L36A)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    WATER (UNII: 059QF0KO0R)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73287-021-011 in 1 CARTON01/14/2022
    1119 g in 1 JAR; Type 0: Not a Combination Product
    2NDC:73287-021-02524 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/22/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/14/2022
    Labeler - TELEBRANDS CORP (177266558)
    Establishment
    NameAddressID/FEIBusiness Operations
    Neutraderm, Inc.146224444manufacture(73287-021)
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