Active Ingredient
Menthol 4.00%
Dr. Carrasco Pain Relief Cream
FDA Label NDC 69921-024
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Carrasco Enterprises, Inc. for the product Dr. Carrasco Pain Relief (NDC 69921-024). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose section, uses, directions, warnings, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 (Box)
* Please review the disclaimer below.
