Active Ingredients
Benzocaine 5%
Benzalkonium Chloride .13%
Makesense
FDA Label NDC 69020-209
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 69020-209). 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, stop use and ask a doctor, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
External Analgesic
External Antiseptic
Uses
■ temporarily relieves itching
Warnings
For external use only
Avoid contact with eyes
Stop Use And Ask A Doctor
■ condition or symptoms worsens ■ symptoms do not improve in 7 days ■ if symptoms clear up and occur again within a few days
Do not apply over large areas of the body
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
■ Adults and children 2 years of age and older: Apply a fingertip amount (approximately 1-inch strip) to affected area not more than 3 to 4 times daily ■ Children under 2 years of age: Consult a doctor
Inactive Ingredients
Cetearyl Alcohol, Diaziolidinyl Urea, Dimethicone, Glyceryl Stearate, Hydroxpropyl Bisstearyldimonium Chloride, Methyparaben, Peg-100 Stearate, Peg-400, Propylparaben, Purified water
Package Label
Image Description (Cfemantitchlbl)
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