Active Ingredient
Benzocaine 20%
The following Structured Product Label (SPL) was submitted to the FDA by Cherry Hill Sales Co for the product Makesense (NDC 69020-207). 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, uses, warnings, do not use, when using this product, stop use and aska doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Benzocaine 20%
Oral Pain Reliever
for the temporary relief of pain associated with:
■ toothache ■ canker sores ■ cold sores ■ fever blisters ■ minor dental procedures
Allergy alert: do not use this product if your child has a history of allergy to local anesthetics such as procaine, butacaine or other "caine" anesthetics
■ more than directed ■ for more than 7 days unless directed by a physician or healthcare provider.
■ fever and nasal congestion are not symptoms of teething and may indicate the presence of infection. If these symptoms persist, consult your physician
■ sore mouth symptoms do not get better in 7 days ■ irritation, pain or redness does not go away ■ swelling, rash or fever develops
In case of overdose or allergic reaction get medical help or contact a Poison Control Center immediately.
Adults and children 2 years of age and older:■ cut open tip of tube ■ apply to affected area up to 4 times daily or as directed by a dentist or physician ■ children under 12 years of age should be supervised using this product ■ for infants under 2 years of age, ask a doctor or health care provider
■ store at 59 to 77F (15-25C) ■ do not use if tube tip is cut prior to opening
Methylparaben, Mineral Oil, Ozocerite, Petrolatum, Propanediol, Propylparaben
* Please review the disclaimer below.