Active Ingredients
Camphor 1%
Menthol 1%
Makesense
FDA Label NDC 69020-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cherry Hill Sales Co for the product Makesense (NDC 69020-201). 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 ingredients, purpose, uses, warnings, do not use, 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
External analgesic
External Analgesic
Uses
For temporary relief of pain and itch associated with ■ dry skin itch ■ insect bites ■ minor cuts & scrapes ■ minor skin irritations
■ sunburn
Warnings
For external use only
Do Not Use
■
■ on wounds or damaged skin ■ with a heating pad ■ on a child under 12 years of age with arthritis-like conditions
When Using This Product
■ avoid contact with the eyes
Stop Use And Ask A Doctor
■ condition worsens or if symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ excessive skin irritation occurs
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
■ adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
■ children under 12 years of age: ask a doctor
Other Information
■ store at 20 to 25C (68 to 77F)
Inactive Ingredients
Alcohol, Aloe Vera, Carbomer, Cetearyl Alcohol, Glycerin, Glyceryl Stearate, Methylparaben, Mineral Oil, Petrolatum, Propylparaben, Purified Water, Steareth-2, Steareth-21, Triethanolamine, Vitamin E.
Package Label
Image Description (Medantiitchlbl)
* Please review the disclaimer below.
