Active Ingredient
Benzocaine (20%), L-Methol (1%)
Medicaine Sting And Bite
FDA Label NDC 68183-118
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Custom Kits Company Inc for the product Medicaine Sting And Bite (NDC 68183-118). 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, otc - purpose, uses, warning, stop use, keep out of reach of children, directions, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
analgesic
Uses
For temporary relief of pain and itching associated with insect bites and stings
Warning
Do not use in the eyes
Not for prolonged use
Stop Use
If condition for this preparatiob is used persists or if a rash or irritation develops
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a poison control center right away
Directions
reverse cardboard sleeve then crish at dot between thumb and forefinger. Once solution has saturated tip, apply to sting or bite.
Other Safety Information
Store at room temperature away from light
Inactive Ingredients
D&C Green Dye #5 D&C Yellow Dye #10, FD&C Blue Dye #1, PEG 300 NF, Isopropyl Alcohol, Purified Water, USP
Package Label.Principal Display Panel
U1-19.jpg (U1 19)
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