Label: ABONIKI BALM - ULTRA STRENGTH TOPICAL PAIN RELIEF BALM - WHITE- camphor, eucalyptus, menthol, methyl salicylate ointment

  • NDC Code(s): 82729-005-01, 82729-005-02
  • Packager: J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 2, 2023

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  • Aboniki® Balm - Ultra Strength Topical Pain Relief Balm - White

  • Drug Facts

    Drug Facts

  • Active Ingredients

    Active Ingredients (In each gram)

    Camphor 4%

    Menthol 16%

    Methyl Salicylate 49%

  • Purpose

    Active Ingredients (In each gram) ​Purpose
    Camphor 4%External Analgesic
    Menthol 16%External Analgesic
    Methyl Salicylate 49%External Analgesic

  • USES

    Temporarily relieves minor aches & pains related to:

    • arthritis
    • simple backaches
    • sore muscles
    • joint pain
    • dislocation
    • leg cramps
    • bruises
    • sprains
  • Warning

    For external use only.

  • Do not use

    • on wounds or damaged skin
    • with a heating pad
    • if you are allergic to any of the ingredients
  • Ask a doctor or pharmacist before use if you have

    • sensitive skin
    • redness over the affected area
  • When using this product

    • avoid contact with eyes and mucous membranes
    • do not bandage tightly
  • Stop use and ask a doctor if

    • rash, itching, or excessive irritation of the skin develops
    • condition worsens or symptoms persist for more than 7 days
    • 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.

  • Direction

    • Use only as directed
    • For adults and children over 12 years, apply to the affected area 3 to 4 times daily
    • Wash hands after use
    • For Children under 12 years, consult a doctor before use
  • Other Information

    • Store in a cool, dry place between 20 oC to 25 oC (68 oF - 77 oF)
    • Do not use if the seal is broken
    • See cap for lot no, mfg, and exp date
  • Inactive Ingredients

    Eucalyptus Oil, Lanolin, Microcrystalline Wax, Paraffin, Petrolatum.

  • Contact Info

    Distributed by:

    J. C. Udeozor & Sons Global Industries Limited

    Email:

    Info-US@aboniki.com

    Mail:

    300 Delaware Ave, Suite 210 #465
    Wilmington, DE 19801

    USA

  • Aboniki ® Balm - Ultra Strength Topical Pain Relief Balm - Twin Pack [Two 25g (0.88 OZ) Jar Inside]

    • Aboniki ® Balm - Ultra Strength Topical Pain Relief Balm - White
    • New Powerful Formula
    • Fast and Deep Penetrating Pain Relief

    ABONIKI Ultra Strength - White 20230822

  • INGREDIENTS AND APPEARANCE
    ABONIKI BALM - ULTRA STRENGTH TOPICAL PAIN RELIEF BALM - WHITE 
    camphor, eucalyptus, menthol, methyl salicylate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82729-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL160 mg  in 1 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE490 mg  in 1 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorMENTHOLImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82729-005-0125 g in 1 JAR; Type 0: Not a Combination Product10/02/2023
    2NDC:82729-005-022 in 1 CARTON10/02/2023
    2NDC:82729-005-0125 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/02/2023
    Labeler - J C UDEOZOR & SONS GLOBAL INDUSTRIES LTD (851768299)
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