Label: TOTALARTHRITIS- camphor, eugenol, menthol ointment

  • NDC Code(s): 73417-852-52
  • Packager: PhytoBiologic Pharmaceutics LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 24, 2021

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

  • TotalArthritis Active Ingredients

    Camphor4%External Analgesic
    Eugenol 4%Anti-Inflammatory
    Menthol 4%External Analgesic

    TotalArthritis DrugFact

    TotalArthritis DrugFact

  • Purpose

    CamphorExternal Analgesic
    EugenolAnti-inflammatory
    MentholExternal Analgesic

    TotalArthritis Cover

  • Uses

    For sustained relief of pain, swelling and Inflammation in joints, muscle and tendon associated with:
    • Acute and chronic rheumatoid arthritis, gout, osteoarthritis and psoriatic arthritis.
    • Chronic back/neck pain due to arthritis, spondylitis.

    TotalArthritis Uses

  • Warnings for external use only

    • Avoid contact with eyes and mucous membranes.
    • Do not apply excessive external heat.
    • Use only as directed.
  • When using this product

    • Do not apply excessive external heat
    • Avoid contact with eyes and mucous membranes.

  • Stop use of this product and consult a doctor If

    • Skin rash occurs

  • If pregnant or breast-feeding, or symptoms persist, consult medical professional before use

  • Keep out of reach of children, if swallowed, get Imrnedlate medical help.

  • Directions

    • Apply a generous amount of the ointment (~1g) on affected area 3 times daily and massage gently. For faster results, apply

    local heat with a heat lamp or heat pad after each application.

    • For chronic severe conditions, use the ointment for 6 to 9 months and as advised by the physician*.

    * Individual results vary depending on the chronic conditions, age and time length of suffering.

  • Other information

    • Store in room temperature 40 0F to 86 0F (4 0C to 30 0C)
    • Bioactive formula has a natural color that can stain cloths
  • Inactive Ingredients

    Aloe vera extract, Azadirachta indica extract, Bees wax,Curcuma longa root extract, Fragrance, Ginger extract, Lemon grass oil, Mustard oil, Nigella sativa extract, Peppermint oil, Petroleum jelly, Rubia cordifolia extract.

  • Questions or Comments ?

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  • Principal Display Panel - 25 g Jar Carton NDC 73417-852-52 TotalArthritis TM Net Wt: 0.90 OZ (25g)

    TotalArthritis 25g Jar Label

  • INGREDIENTS AND APPEARANCE
    TOTALARTHRITIS 
    camphor, eugenol, menthol ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73417-852
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)40 mg  in 1 g
    EUGENOL (UNII: 3T8H1794QW) (EUGENOL - UNII:3T8H1794QW) EUGENOL40 mg  in 1 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    NIGELLA SATIVA SEED (UNII: 4LVZ0Z0ITT)  
    EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)  
    MUSTARD OIL (UNII: TYY1MA9BSY)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    AZADIRACHTA INDICA LEAF (UNII: HKY915780T)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    RUBIA CORDIFOLIA ROOT (UNII: 4V873H15CG)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TURMERIC (UNII: 856YO1Z64F)  
    GINGER (UNII: C5529G5JPQ)  
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73417-852-521 in 1 CARTON08/12/2021
    125 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34808/12/2021
    Labeler - PhytoBiologic Pharmaceutics LLC (117103844)
    Registrant - PhytoBiologic Pharmaceutics LLC (117103844)
    Establishment
    NameAddressID/FEIBusiness Operations
    PhytoBiologic Pharmaceutics LLC117103844manufacture(73417-852) , label(73417-852)