Label: PAIN CREAM- analgesic cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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

  • Active Ingredient

    Menthol 6%

    Camphor 5%

    Purpose

    Topical Analgesic

  • Uses:

    For Temporary relief of aches and pains of muscles and joints associated with arthritis, bachaches, strains, or sprains.

  • WARNINGS:

    For external use only. Do not use if safety seal is damaged or missing.

  • WHEN USING THIS PRODUCT

    Use only as directed: Avoid contact with eyes or mucous membranes: Do not apply directly to wounds or damaged skin: Do no use in combination with other ointments, creams, or sprays: Wash hands with cool water after each use: Do not sue with a heat pad or device.

  • Stop Usage immediately and as a doctor if:

    Condition worsens or symptoms persist for more than 7 days.

  • If pregnant or breast-feeding:

    Ask a health professional before use

  • Keep out of reach of children

    If ingested, get medical help, or contact poison control center immediately: 1-800-222-1222

  • Directions:

    Adults and children over 12 years old: Apply to affected area - do not apply more than 4 times adaily: Children 12 years or younger: Consult a doctor

  • Other Information

    Flammable: Keep away from excessive heat or open flame. Keep out of direct sunlight: Store at 50-86F (15-30C)

  • Inactive Ingredients:

    Bis-Vinyl Dimethicone/Dimthicone Copolymer, C13-C14 Isoparaffin, Caprylic/Capric Triglyceride, Cetyl Alcohol, Dimethicone, Glyceryl Stearate, Glycol Stearate, Jojoba Oil, Laureth-7, Lavender Oil, Phenoxyethanol, Polyarylamide, Shea Butter, Simethicone, Sodium Acrylate/Sodium Acrylol Dimethyl Taurate Copolymer, Spearmint Oil, Water.

  • INSTA EAZE: RUB THE PAIN AWAY

    Insta Eaze Rub The Pain Away

  • INGREDIENTS AND APPEARANCE
    PAIN CREAM 
    analgesic cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79804-260
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.06 g  in 1 g
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.05 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CETYL DIMETHICONE/BIS-VINYLDIMETHICONE CROSSPOLYMER (UNII: AE7QA6TW0Q)  
    CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)  
    WATER (UNII: 059QF0KO0R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    LAURETH-7 (UNII: Z95S6G8201)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    SPEARMINT OIL (UNII: C3M81465G5)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    JOJOBA OIL (UNII: 724GKU717M)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79804-260-0259 g in 1 PACKAGE; Type 0: Not a Combination Product08/22/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/22/2022
    Labeler - Eagle Labs Inc. (118496872)
    Registrant - Eagle Labs Inc (118496872)
    Establishment
    NameAddressID/FEIBusiness Operations
    Eagle Labs Inc118496872manufacture(79804-260) , pack(79804-260) , label(79804-260)