Label: DR. CARRASCO PAIN RELIEF- menthol cream

  • NDC Code(s): 69921-024-01
  • Packager: Carrasco Enterprises, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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

View All Sections
  • Drug Facts

  • Active Ingredient

    Menthol 4.00%

    Purpose Section

    External Analgesic

  • Uses

    For temporary relief of minor aches and pains associated with backache, arthritis, bruises, sprains and strains.

  • Directions

    Apply directly to affected area. Do not use more than four times per day.

  • Warnings

    For external use only.

    When using this product

    keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctor

    if rash or irritation develops and last.

    Keep out of reach of children.

    If swallowed , get medical help or contact your local poison Control Center or emergency room immediately.

  • Inactive Ingredients

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arctium Lappa (Burdock) Root Extract, Arnica Montana (Arnica) Extract, Boswella Serrata Extract, Calendula Officianalis (Marigold) Flower Extract, Camellia Sinensis (Green Tea) Leaf Extract, Camphor, Carbomer, Citrus Medica Limonum (Lemon) Peel Oil, Dmdm Hydantoin, Isopropyl Alcohol, Mentha Viridis (Spearmint) Extract, Sodium Hydroxide, Tocopheryl Acetate (Vitamin E).

  • Product Label

    Box

  • INGREDIENTS AND APPEARANCE
    DR. CARRASCO PAIN RELIEF 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69921-024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    ARNICA MONTANA (UNII: O80TY208ZW)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MENTHA SPICATA (UNII: O2H83I4PUN)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69921-024-011 in 1 CARTON02/06/2017
    189 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/21/2015
    Labeler - Carrasco Enterprises, Inc. (079850370)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!