Label: VELTRIX- veltrix pain relieiving cream cream

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated July 13, 2015

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  • INFORMATION FOR PATIENTS

    PURPOSE: Topical analgesic


    ACTIVE INGREDIENTS
    Lidocain 4% --------------------------------------------------------------------------------------------------------- Topical analgesic
    Menthol 1% --------------------------------------------------------------------------------------------------------- Topical analgesic

  • INDICATIONS & USAGE

    INDICATIONS
    For the temporary relief of pain of muscles and joints associated with:

    • Arthritis
    • Simple Backache
    • Strains
    • Sprains
    • Bruises

    DIRECTIONS
    Adults and children over 12 years
    Apply generously to affected area
    Massage into painful area until thoroughly absorbed into skin, repeat as necessary, not more than 3-4 times daily
    Store at 20°-25°C (68°-77 °F). Avoid direct sunlight.

  • WARNINGS

    WARNINGS
    FOR EXTERNAL USE ONLY.

    • When using this product use only as directed
    • Do not bandage tightly
    • Do not use with a heating pad
    • Agoid contact with the eyes or mucous membranes
    • Do not apply to wounds or damaged or irritated skin
  • WARNINGS AND PRECAUTIONS

    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
    • Irritation develops
  • OTHER SAFETY INFORMATION

    • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
    • If pregnant of breast-feeding, ask a healthcare professional before use
  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS
    aliphatic alcohol; stearic acid; vaseline; peregal; Carmellose; odium; water

  • PRINCIPAL DISPLAY PANEL

    VeltrixRX.jpg

  • INGREDIENTS AND APPEARANCE
    VELTRIX 
    veltrix pain relieiving cream cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69379-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69379-004-03120 g in 1 BOTTLE; Type 0: Not a Combination Product07/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2015
    Labeler - Home Aide Diagnostics, Inc. (783518983)
    Registrant - Zhejiang Bangli Medical Products Cl. Ltd. (421295875)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Bangli Medical Products Cl. Ltd.421295875manufacture(69379-004)
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