Label: HEMPVANA MAXIMUM STRENGTH PAIN RELIEF- trolamine salicylate lotion

  • 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 February 28, 2022

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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 using roller ball applicator
    • Children under 2 years of age: consult a physician
  • Inactive Ingredients

    Water/Aqua/Eau, Ethylhexyl Stearate, Butylene Glycol, Caprylic/Capric Triglyceride, Dimethicone, Cannabis Sativa (Hemp) Seed Oil, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Stearic Acid, Tocopheryl Acetate, Allantoin, Phenoxyethanol, Xanthan Gum, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Disodium EDTA, Citric Acid, Sodium Hydroxide

  • Questions?

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

  • PRINCIPAL DISPLAY PANEL

    #1 Hemp Pain Relief Brand in America 1

    1AC Nielsen 2021 food drug mass POS

    Hempvana Brand

    Maximum Strength Pain Relief Lotion

    Odor Free!

    New! 5 Deep Massaging Stainless Steel Rollerballs

    Original

    +Hemp Seed Oil

    For Moisturization

    Trolamine Salicylate 10% For Pain

    Net Wt. 2.5 OZ (71 g)

    1

  • INGREDIENTS AND APPEARANCE
    HEMPVANA MAXIMUM STRENGTH PAIN RELIEF 
    trolamine salicylate lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73287-022
    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
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    ALLANTOIN (UNII: 344S277G0Z)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73287-022-011 in 1 CARTON02/28/2022
    171 g in 1 APPLICATOR; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34802/28/2022
    Labeler - TELEBRANDS CORP (177266558)
    Establishment
    NameAddressID/FEIBusiness Operations
    Neutraderm, Inc.146224444manufacture(73287-022)
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