MEDI-FIRST Topical Analgesic
Lidocaine HCI · Spray · Topical
Active ingredient
Active ingredient Lidocaine HCI 2.0%
Purpose
Purpose Topical pain relief
Uses
Uses Temporary pain relief associated with minor burns
Warnings
Warnings For external use only.
Do not use
Do not use in large quantities, particularly over raw or blistered areas near eyes, if this happens rinse thoroughly with water
Stop use and ask a doctor
Stop use and ask a doctor if condition worsens or persists for more than 7 days or clears up and returns.
Keep out of reach of children
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions spray an even layer of burn spray over cleaned affected area not more than 3-4 times daily not to be used on Children under 12 years of age
Inactive ingredients
Inactive ingredients aminomethyl propanol, glycerin, hydroxypropyl methylcellulose, melaleuca alterniflia (tea tree) leaf oil, octoxynol 9,PEG-40 hydrogenated castor oil, phenoxyethanol, propylene glycol, water
Questions?
Questions or comments? 1-800-634-7680
Label text from the FDA structured product label by Ultra Distributors Inc (revised Sep 7, 2026). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Lidocaine Hydrochloride in 1 product
MEDI-FIRST Topical Analgesic NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 78495-142 | Lidocaine Hydrochloride 20 mg/mL Spray | Ultra Distributors Inc | OTC MONOGRAPH DRUG |
Frequently asked questions
What is MEDI-FIRST Topical Analgesic used for?
Uses Temporary pain relief associated with minor burns
Who makes MEDI-FIRST Topical Analgesic?
MEDI-FIRST Topical Analgesic is listed by 1 labeler in the FDA NDC directory, including Ultra Distributors Inc.