Label: ALLG PAIN RELIEF FAST ACTING PAIN (camphor- synthetic 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 January 24, 2022

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Camphor 5%

  • Purpose

    External Analgesic

  • Uses

    • minor arthritis pain
    • simple backache
    • muscle sprains
    • bruises
    • muscle strains
    • cramps
  • Warnings

    For external use only

    Do not use if

    • skin is irritated or damaged
    • excessive irritation develops
    • 12 years of age or under

    When using this product avoid contact with the eyes and mucous membranes

    • do not apply to wounds, damaged, broke or irrated skin
    • do not bandage tightly or use a heating pad
    • do not swallow If swallowed, contact a physician or contact a poison control center immediately

    Stop and ask doctor if

    • condition worsens
    • symptoms persist for more than 7 days or clear up and occur again within a few days
    • redness develops

    If pregnant or breastfeeding, ask a health professional before use.

    Keep out of reach of children

  • Directions

    • clean, rinse, and dry skin prior to application
    • apply generously to painful muscles and joints, gently massaging until the ALLG® Pain Relief Fast- Acting Pain Cream disappears
    • repeat as necessary, but no more than four times a day
    • for optimum benefit, use daily for at least two weeks
  • Other

    • store at room temperature with the cap closed
    • Notice: because this product contains natural nutrients color may vary
  • Inactive Ingredients

    Acrylate/C10-30 Alkyl Acrylate Crosspolymer, Aescin (Horse Chestnut Extract), Aloe Vera, Arnica Montana Extract, C12-15 Alkyl Benzoate, Cannabis Sativa Extract (Hemp Derived), Chondroitin Sulfate, Diazodinyl Urea, Dimethicone, Disodium EDTA, dl Panthenol, Fructoborate, Glucosamine Sulfate, Glycerin, Glycerol Stearate, Hydroxypropyl Methylcellulose, Iodopropynyl Butylcarbamate, Methyl Gluceth-20, Methyl Glucose Sesquistearate, Peppermint Oil, Polysorbate 20, Potassium Carbomer, Purified Water, Shea Butter, Tocopheryl Acetate, Trolamine Salicylate

  • Questions or comments?

    Call (877) 383-2334

  • PRINCIPAL DISPLAY PANEL - 114 g Jar Label

    NET WT 4 OZ. (114g)

    ALL G®
    ESSENTIALS
    200MG
    CBD

    PAIN RELIEF +
    FAST-ACTING PAIN CREAM
    BROAD SPECTRUM CBD

    GOOD FOR
    INJURY
    PAIN
    RELAXATION
    COMFORT
    SOOTHING

    PRINCIPAL DISPLAY PANEL - 114 g Jar Label
  • INGREDIENTS AND APPEARANCE
    ALLG PAIN RELIEF   FAST ACTING PAIN
    camphor (synthetic) cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72593-155
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)5 mg  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    Methyl Glucose Sesquistearate (UNII: V1YW10H14D)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARNICA MONTANA WHOLE (UNII: O80TY208ZW)  
    CALCITRIOL (UNII: FXC9231JVH)  
    CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)  
    Diazolidinyl Urea (UNII: H5RIZ3MPW4)  
    Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Escin (UNII: RUU8G67GQM)  
    GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N)  
    Glycerin (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    Methyl Gluceth-20 (UNII: J3QD0LD11P)  
    Peppermint Oil (UNII: AV092KU4JH)  
    Potassium Hydroxide (UNII: WZH3C48M4T)  
    WATER (UNII: 059QF0KO0R)  
    Shea Butter (UNII: K49155WL9Y)  
    Sorbitan Monolaurate (UNII: 6W9PS8B71J)  
    Trolamine Salicylate (UNII: H8O4040BHD)  
    Cannabidiol (UNII: 19GBJ60SN5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72593-155-13114 g in 1 JAR; Type 0: Not a Combination Product09/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34809/28/2020
    Labeler - Global Products Group, LLC (081371764)
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