Label: SANAR NATURALS ARNICA PAIN RELEIVING ROLL ON WITH CAMPHOR- camphor liquid

  • NDC Code(s): 73386-148-03
  • Packager: Sanvall Enterprises, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 31, 2024

If you are a consumer or patient please visit this version.

  • Active ingredient

    Camphor 1%

    Purpose

    Pain Relief

  • Uses

    For the temporary relief of minor aches and pains of muscles joints

  • Warnings

    For external use only

    Avoid contact with eyes.

    Do not

    use on wounds or damaged skin

    bandage tightly

    Stop use and ask a doctor if

    condition worsens, or if symptoms persist for more than 7 days or clear up and occur again.

    Keep out of reach of children.

    is swallowed, get medical help or contact Poison Control Center right away

  • Directions

    • Adults and children over 12 years: Apply to affected area no more than 3 to 4 times daily.
    • Children under 12 years: Do not use, consult a doctor.
  • Other Information

    Store tightly closed in a dry place at controlled room temperature between 59-77 F (15-25 C)

  • Inactive ingredients

    Aqua, Arnica Montana Flowe Extract, Propylene Glycol, Menthol, Glycerin, Carbomer, Methyl Salicylate, Ththanolamine, Eucalyptus Globulus Leaf Oil, Disodium EDTA, Tocopheryl Acetate, Capsicum Annum Fruit Extract, Methylchloroisothiazolinone, Methylisothiazolinone.

  • Label copy

    label

  • INGREDIENTS AND APPEARANCE
    SANAR NATURALS ARNICA PAIN RELEIVING ROLL ON WITH CAMPHOR 
    camphor liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73386-148
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    CAPSICUM FRUTESCENS WHOLE (UNII: 6XJX33L87P)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MENTHOL (UNII: L7T10EIP3A)  
    CARBOMER 980 (UNII: 4Q93RCW27E)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73386-148-0388.5 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/01/2024
    Labeler - Sanvall Enterprises, Inc (966905507)
    Establishment
    NameAddressID/FEIBusiness Operations
    Evi Labs123617598manufacture(73386-148)