Label: ARCTIC BLAST PAIN RELEIVING (menthol, camphor- synthetic liquid

  • NDC Code(s): 71856-176-01
  • Packager: Nutriomo Labs Pte, Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 10, 2025

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  • Drug Facts

  • Active ingredients

    Menthol 10.00%

    Camphor 3.00%

    Purpose

    Topical Analgesic

  • Indications:

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

  • Warnings

    • For external use only.
    • Use only as directed.

    Flammable

    • Keep away from fire, flame, sparks and heated surfaces.
    • Tighten cap firmly.

    Stop use and ask doctor if

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

    When using this product

    • avoid contact with the eyes
    • do not apply to wounds or damaged skin
    • do not bandage tightly

    If pregnant or breat-feeding,

    ask a health professional before use.

    Keep out of reach of children.

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

  • Directions

    For adults: Apply to affected area no more than 3 to 4 times daily.

  • Other Information

    • Store product at room temperature
    • Do not use if printed safety seal on cap is broken or missing
  • Inactive Ingredients

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Calendula Officinalis Extract, Dimethyl Sulfoxide (DMSO), Emu Oil, Ethylhexylglycerin, Glycerin, Hypericum Perforatum (St. John's Wort), Isopropyl Alcohol, Methyl Salicylate, Olea Europaea (Olive) Oil, Phenoxyethanol, Polysorbate-20, Propylene Glycol, SD-Alcohol 40B.

  • Questions?

    Call 1-800-856-5587

  • Package Labeling:

    Label0

  • INGREDIENTS AND APPEARANCE
    ARCTIC BLAST PAIN RELEIVING 
    menthol, camphor (synthetic) liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71856-176
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL100 mg  in 1 mL
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
    EMU OIL (UNII: 344821WD61)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71856-176-0130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product05/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/01/2018
    Labeler - Nutriomo Labs Pte, Ltd (659264720)
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