Label: CVS ARTHRITIS PAIN RELIEF- arthritis pain relief cream

  • 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 August 31, 2016

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

  • SPL UNCLASSIFIED SECTION

    Drug facts

  • Active Ingredient

    Histamine Dihydrochloride .025%

  • Purpose

    Topical Analgesic

  • Use

    For temporary relief of minor aches and pains of muscles and joints assited with arthritis, simple backache, strains & bruises.

  • Warnings

    For external use only.

    Do not use on wounds or damaged skin or if you are allergic to ingredients in the product.

  • When using this product

    Avoid contact with eyes. If product gets inot eyes,rinse thoroughly with water.

    Do not bandage tightly or use a heating pad.

  • Stop use and ask a doctor if

    Rash appears.

    Condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and occur again within a few days.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    For use by adults and Children over 12 years of age.

    • apply a thin layer tp the pain site and massage until thoroughly absorbed into skin. Apply no more than 3 to 4 times daily.
    • Children 12 years or younger consult a physician.
  • Other information

    Store between 68° and 77° F ( 20° and 25° C)

    Tamper evident feature:do not use if outer shrink wrap on jar is torn, broken or missing.

  • Inactive Ingredients

    Deoinized Water, Emu Oil, Butylene Glycol, Polyacrylamide, Sodium Polyacrylate, C13-C14 Isoparaffin, Laureth-7, Methylsulfonylmethane, Hellanthus Annuus( Sunflower )Oil, Ethylhexyl Stearate, Glucosamine HCL, Chondroitin Sulfate, Tocopheryl Acetate, Trideceth-6, Tetrasodium EDTA, Potassium Sorbate, Methylisothiazolinone

  • CVS Arthritis Cream 4 oz-jar

    CVS Arthritis Cream 4 oz-jar

    CVS Health

    Arthritis Pain Relief Cream

    Histamine Dihydrochloride

    Soothes muscle and joint pain

    NET WT 4 oz (113g)

  • CVS Arthritis Cream 4 oz -Carton

    CVS Arthritis Cream 4 oz -Carton

    CVS Health

    Arthritis Pain Releif Cream

    Histamine Dihydrochloride

    Soothes muscle&joint pain

    • Odor and burn free
    • Moisturizing formula
    • Also contains emu oil, MSM, glucosamine & chondroitin         NET WT 4oz (113g)
  • INGREDIENTS AND APPEARANCE
    CVS ARTHRITIS PAIN RELIEF 
    arthritis pain relief cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE.025 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    EMU OIL (UNII: 344821WD61)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    LAURETH-7 (UNII: Z95S6G8201)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)  
    CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-301-601 in 1 CARTON05/30/2016
    1113 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 finalpart34805/30/2016
    Labeler - CVS Health (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sheffield Pharmaceuticals LLC151177797manufacture(69842-301)