Label: NEURITRX- capsaicin 0.075% cream

  • 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 24, 2019

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

  • Active Ingredient

    Capsaicin 0.075%

  • Purpose

    Topical Analgesic

  • Uses

    For the temporary relief of minor aches and pains of muscles and joints associated with:
    • simple backache

    • arthritis

    • strains

    • bruises

    • sprains

  • Warnings

    For external use only

  • When using this product

    • use only as directed
    • do not bandage tightly
    • do not use with heating pad
    • avoid contact with eyes and mucous membranes
    • do not apply to wounds, damaged, broken or irritated skin
    • a transient burning sensation may occur upon application but generally disappears in several days
    • if severe burning sensation occurs, discontinue use immediately
    • do not expose the area treated with product to heat or direct sunlight

  • Stop use and ask a doctor if

    • Condition worsens

    • Redness is present

    • Irritation develops 

    • Symptoms persist for more than 7 days or symptoms clear up and occur again within a few days

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Adults and children over 18 years:

    • Apply to affected area
    • Massage into painful area until thoroughly absorbed
    • Repeat as necessary, but no more than 3 to 4 times daily


    Children 18 years or younger: ask a doctor

  • Other Information

    Store at 20° - 25°C (68° - 77°F)

    Do not use if inner container seal is damaged or missing.

  • Inactive Ingredients

    Almond Oil, Benzyl Alcohol, Benzyl Benzoate, Butylated Hydroxytoluene, Carbomer Copolymer Type B, Cinnamon Bark Oil, Coriander Oil, Edetate Disodium, Isopropyl Alcohol, L-Arginine HCl, L-Citrulline , Polyoxl 40 Hydrogenated Castor Oil, Propylene Glycol, Sorbitol,Trolamine, Water

  • Neuritrx carton

    image description

  • INGREDIENTS AND APPEARANCE
    NEURITRX 
    capsaicin 0.075% cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72826-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN.075 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALMOND OIL (UNII: 66YXD4DKO9)  
    ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    CITRULLINE (UNII: 29VT07BGDA)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    CORIANDER OIL (UNII: 7626GC95E5)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SORBITOL (UNII: 506T60A25R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72826-102-141 in 1 CARTON11/29/2019
    156.7 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34811/29/2019
    Labeler - Semprae Laboratories Inc (093739668)
    Registrant - Semprae Laboratories Inc (093739668)
    Establishment
    NameAddressID/FEIBusiness Operations
    Topical Pharmaceuticals Inc.831530683manufacture(72826-102)