Label: HISTAMINE DIHYDROCHLORIDE cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 1, 2023

If you are a consumer or patient please visit this version.

  • Broadway Joe's Pain Cream

    Histamine dihydrochloride

  • Braodway Joe's Pain Cream

    Water, Glyceryl Stearate, Caprylic/Capric, Triglyceride, Cetyl Alcohol, Butylene Glycol, Cannabidiol, Cetearyl 2- thylhexanoate, Sodium Hyaluronate, Glycerin, Tapioca Starch, Polymethylsilsesquioxane, Stearic Acid, Cannabis Sativa (Hemp) Seed Oil, 3-glyceryl Ascorbate (Vitamin C), Isonononyl Isononanoate, Tocopheryl Acetate (Vitamin E), Dimethicone, Polysorbate 80, Carbomer, Sodium Hydroxide, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol

  • Broadway Joe's Pain Cream

    • For use by adults and children over 13 yrs old.
    • Gently massage the product on to clean dry skin as needed.
    • For topical use only, do not ingest.
    • Provides temporary relief from aches and pains associated with simple backaches,strains, sprains, arthritis, bruises.
    • Apply a thin layer to pain site and massage until thoroughly absorbed into skin.
  • Broadway Joe's Pain Cream

    Topical Analgesic

  • Broadway Joe's Pain Cream

    Store between 40 degrees F and 86 degrees F (4 degrees C and 30 degrees C).

  • Broadway Joe's Pain Cream

    Warnings · For external use only.
    Do not use on open wounds or damaged skin or with a heating pad.


    When using this product · avoid contact with eyes or mucous membranes. If product contacts your eyes, rinse thoroughly with water. Do not bandage tightly. · Do not use with other ointments, creams, or sprays.


    Stop use and ask a doctor if you experience redness or excessive skin irritation over the affected area. · If the condition worsens, or symptoms persist for more than 7 days please consult a Dr.


    Keep out of reach of children. If swallowed, seek medical help, or contact a Poison Control Center immediately.


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

  • Broadway Joe's Pain Cream

    Stop use and ask a doctor if you experience redness or excessive skin irritation over the affected area. · If the condition worsens,
    or symptoms persist for more than 7 days, please consult a Dr.

  • Broadway Joe's Pain Cream

    Side label and Drug Fact

  • Broadway Joe's Pain Cream

    Keep out of reach of children. If swallowed, seek medical help or contact a poison control center immediately.

  • Broadway Joe's Pain Cream

    Side label plus Drug Fact

  • INGREDIENTS AND APPEARANCE
    HISTAMINE DIHYDROCHLORIDE 
    histamine dihydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83088-8120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE0.00025 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DIMETHICONE 350 (UNII: 2Y53S6ATLU)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    3-GLYCERYL ASCORBATE (UNII: 3R1Q5X5GGO)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)  
    ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL DICAPRATE (UNII: 3Z317CA098)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Product Characteristics
    Colorwhite (Cream) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83088-8120-814.8 mL in 1 JAR; Type 0: Not a Combination Product02/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/01/2023
    Labeler - USA Hemp Store LLC (036959608)
    Registrant - Lexia LLC (050186540)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lexia LLC015552120manufacture(83088-8120)