Label: GERMA MANTECA UBRE PLUS (TIN)- methyl salicylate 10% ointment

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

Drug Label Information

Updated October 19, 2023

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  • Active Ingredient

    Methyl Salicylate 10%

  • Uses

    For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, strains, sprains, arthritis and sports injuries.

  • INDICATIONS & USAGE

    Clean skin of lotions, creams, ointments, liniment or sprays ■ Apply liberally to affected area and massage until absorbed into skin ■ Do not apply more than 3 or 4 times daily. ■ Children under 12 years of age, ask a doctor.

  • Purpose

    Topical Analgesic

  • Warnings

    For external use only ■ Use only as directed

    Do not use • on children • with a heating pad • with a tight bandage • on eyes, mucous membranes, wound or irritated skin • over extensive areas of the body.

  • Warnings

    KEEP OUT OF THE REACH OF CHILDREN

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • PREGNANCY OR BREAST FEEDING

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

  • ASK DOCTOR

    Consult a doctor and discontinue use • If condition worsens or symptoms persist for more than 7 days • If you have sensitive skin • if prone to allergic reaction from any of the ingredients.

  • Other Information

    Store at controlled room temperature 15-30ºC (59-86ºF)

  • Directions

    Clean skin of lotions, creams, ointments, liniment or sprays • Apply liberally to affected area and massage until absorbed into skin • Do not apply more than 3 or 4 times daily. • Children under 12 years of age, ask a doctor.

  • Inactive Ingredients

    Camphor, D&C Color Yellow #11, Eucalyptus Oil, Lanolin Oil, Menthol, Mineral Oil, Paraffin Wax, Propylparaben, Tea Tree Oil, White Petrolatum.

  • Principal Display Panel

    Ubre Plus Tin

  • INGREDIENTS AND APPEARANCE
    GERMA MANTECA UBRE PLUS (TIN) 
    methyl salicylate 10% ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73635-5805
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
    D&C YELLOW NO. 11 (UNII: 44F3HYL954)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    MENTHOL (UNII: L7T10EIP3A)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    LANOLIN OIL (UNII: OVV5IIJ58F)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73635-5805-385.5 mL in 1 CAN; Type 0: Not a Combination Product03/29/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01403/29/2019
    Labeler - Germa Products, LLC (116626935)