Label: SORE NO MORE WARM THERAPRY PLUS CBD 2000MG- menthol camphor gel

  • 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 May 23, 2022

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  • ACTIVE INGREDIENTS

    MENTHOL USP 3%, CAMPHOR USP 3%

  • PURPOSE

    PURPOSE

    EXTERNAL ANALGESIC

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • USES

    TEMPORARILY RELIEVES MINOR ACHES AND PAINS OF MUSCLES AND JOINTS ASSOCIATED WITH: SIMPLE BACKACHES

  • WARNINGS SECTION

    FOR EXTERNAL USE ONLY. DO NOT USE ON WOUNDS OR DAMAGED SKIN. WHEN USING THIS PRODUCTS: AVOID BANDAGING TIGHTLY, AVOID CONTACT WITH EYES, KEEP OUT OF REACH OF CHILDREN.

    STOP USE AND ASK DOCTOR IF: CONDITION WORENS, SYMPTONS PERSIST FOR MORE THAN 7 DAYS, CLEAR UP AND OCCUR AGAIN WITHIN A FEW DAYS.

  • DIRECTIONS

    ADULTS AND CHILDREN 2 YEARS OF AGE AND OLDER: APPLY TO AFFECTED AREA NOT MORE THAN 3 TO 4 TIMES DAILY, RUB IN THOROUGHLY UNTIL GEL IS ABSORBED, CHILDREN UNDER 2 YEARS OF AGE: CONSULT A DOCTOR.

  • INACTIVE INGREDIENTS

    aloe barbadensis leaf juice, carbomer, decyl glucoside, water, citrus grandis (grapefruit) seed extract, camellia sinensis (green tea) leaf extract, citrus aurantium dulcis (orange) peel oil, spiraea ulmaria flower (queen of the prairie) extract, rosa damascena flower water, sodium carbonate, glycerin, hamamelis virginiana (witch hazel) leaf extract, yucca schidigera root extract, phenoxyethanol, caprylyl glycol, cannabidiol, capsicum annuum fruit extract,

  • Question or comments

    1-800-225-3963

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SORE NO MORE WARM THERAPRY PLUS CBD 2000MG 
    menthol camphor gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61577-7012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)0.03 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    DECYL GALLATE (UNII: GJW1U497V5)  
    water (UNII: 059QF0KO0R)  
    CAPSAICIN (UNII: S07O44R1ZM)  
    GRAPE SEED OIL (UNII: 930MLC8XGG)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)  
    ROSA CENTIFOLIA FLOWER OIL (UNII: H32V31VMWY)  
    SODIUM CARBONATE (UNII: 45P3261C7T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    YUCCA SCHIDIGERA ROOT (UNII: E2H9ET15AT)  
    ORANGE PEEL (UNII: TI9T76XD44)  
    CANNABIDIOL (UNII: 19GBJ60SN5)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61577-7012-5113.4 g in 1 JAR; Type 0: Not a Combination Product05/23/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34805/23/2022
    Labeler - SOMBRA COSMETICS INC. (097464309)
    Establishment
    NameAddressID/FEIBusiness Operations
    SOMBRA COSMETICS INC.097464309manufacture(61577-7012) , label(61577-7012)
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