Drug Facts
Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Unifirst First Aid Corporation for the product Medi First Extra Strength Itch Relief (NDC 47682-865). 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 drug facts, active ingredient, purpose, uses, warnings, do not use, ask a doctor before use, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Active Ingredient
Diphenhydramine Hydrochloride 2%
Zinc Acetate 0.1%
Purpose
Topical Analgesic
Skin Protectant
Uses
Warnings
For external use only.
Do not use
Ask a doctor before use
Stop use and ask a doctor if
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Other information
Inactive ingredients
Carbomer homopolymer type C, cetyl alcohol, glycerin, glyceryl monostearate, light mineral oil, methyparaben, polysorbate 60, proplyparaben, purified water, stearic acid
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Medi ♥ First
Topical Solutions
healingmade easy
NDC #47682-865-29
Extra Strength Itch Relief
Temporary relief from pain and itching caused by
insect bites, minoir burns, sunburn, rashes due to
poison ivy, oak, sumac and more
*Compare to the
Active Ingredients
in Extra Strength
Benadryl® Cream
* Please review the disclaimer below.