Label: 7TH MANNA PAIN RELIEF DROPS (menthol, camphor- synthetic liquid

  • NDC Code(s): 71856-423-00
  • Packager: 7TH MANNA (USA) PTE. LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

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  • Drug Facts

  • Active Ingredients

    Menthol 10%

    Camphor 3%

    Purpose

    Topical Analgesic

  • Uses

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

    • arthritis
    • sprains
    • strains
    • bruises
    • simple backaches
  • Warnings

    For external use only.

    Use only as directed.

    Flammable

    • keep away from fire, flame, sparks and heated surfaces
    • tighten cap firmly

    When using this product

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

    Stop use and ask a doctor if

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

    If pregnant or breast-feeding,

    ask a healthcare provider 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 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, Emu Oil, Dimethyl Sulfoxide (DMSO),Ethylhexylglycerin, HypericumPerforatum (St.John's Wort),Isopropyl Alcohol, Methyl Salicylate (Wintergreen) Oil, Olea Europaea (Olive) Oil, Phenoxyethanol, Polysorbate-20, SD-Alcohol 40B.

  • Questions?

    Call us at 1-800-230-8055

  • Package Labeling:

    Outer Package

  • INGREDIENTS AND APPEARANCE
    7TH MANNA PAIN RELIEF DROPS 
    menthol, camphor (synthetic) liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71856-423
    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
    GREEN OLIVE (UNII: 6HD2W46UEG)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    EMU OIL (UNII: 344821WD61)  
    DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HYPERICUM PERFORATUM WHOLE (UNII: XK4IUX8MNB)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71856-423-001 in 1 BOX09/25/2023
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM017B09/25/2023
    Labeler - 7TH MANNA (USA) PTE. LTD. (659264720)
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