Label: MUSCLE AND JOINT RELIEF- emu cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated March 22, 2020

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  • ACTIVE INGREDIENTS

    EMU OIL.....1 X

  • PURPOSE

    PAIN RELIEF

  • WARNINGS

    FOR EXTERNAL USE ONLY.

    DO NOT USE IN EYES.

    CONSULT PHYSICIAN IF SYMPTOMS WORSEN OR CONDITIONS PERSISTS.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL INGESTION, CONSULT YOUR PHYSICIAN OR POISON CONTROL.

  • USES

    NATURAL RX LLC CREAM WILL PENETRATE DEEP INTO JOINTS AND MUSCLES TO RELIEVE PAIN.

  • DIRECTIONS

    APPLY 2 TO 3 TIMES A DAY.

  • INGREDIENTS:

    PURIFIED WATER, ALOE OIL, COCONUT OIL, SWEET ALMOND OIL, CETYL ALCOHOL, STEARYL ALCOHOL, GLYCERYL STEARATE, PEG-75 STEARATE, STEARETH 20, GLYCERIN, PROPYLENE GLYCOL, CAPRYLIC/CAPRIC TRIGLYCERIDES, VITAMIN A, D & E, SHEA BUTTER, D-GLUCOSAMINE HCL, MSM, CHONDROITIN SULFATE, ISOPROPYL MYRISTATE, BEESWAX, DMDM HYDANTOIN.

  • PRINCIPAL DISPLAY PANEL

    MUSCLE-JOINE PAIN_LABEL

  • INGREDIENTS AND APPEARANCE
    MUSCLE AND JOINT RELIEF 
    emu cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69170-104
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EMU OIL (UNII: 344821WD61) (EMU OIL - UNII:344821WD61) EMU OIL1 [hp_X]  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-75 STEARATE (UNII: OT38R0N74H)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    CHONDROITIN SULFATE (CHICKEN) (UNII: 7VZ9466BAB)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69170-104-14118 mL in 1 TUBE; Type 0: Not a Combination Product11/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic11/01/2015
    Labeler - NATURALRX LLC (152081183)
    Establishment
    NameAddressID/FEIBusiness Operations
    DIVERSIFIED MANUFACTURING CORP185073996manufacture(69170-104)
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