Fire Out
Benzocaine and Menthol · Solution · Topical
Active ingredient
Active ingredient Benzocaine USP 20% Menthol USP 1%
Purpose
Purpose (for pain) Topical Anesthetic (anti-itch) Antipruritic
Uses
Uses ▪ Temporarily relieves pain and itching of fire ant bites and stings, insect bites and stings, and minor skin irritation.
Warnings
Warnings ▪ For external use only ▪ Do not apply over large areas of the body ▪ Avoid contact with eyes, mouth, and mucous membranes
Keep out of reach of children
Keep Out of Reach of Children If swallowed get medical help or contact Poison Control Center right away.
Directions
Directions Children under 2 yrs. ▪ Do not use ▪ Consult doctor Adults and children 2 yrs. and older ▪ Clean area ▪ Apply to affected area as needed not more than 3 to 4 times a day.
Inactive ingredients
Inactive Ingredients FD&C Blue #1, Isopropyl Alcohol 15%, PEG-8 Laurate, Water.
Label text from the FDA structured product label by Randob Ltd. (revised Apr 12, 2019). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Benzocaine in 1 product
- Menthol, Unspecified Form in 1 product
Fire Out NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 52412-300 | Benzocaine 200 mg/mL; Menthol, Unspecified Form 10 mg/mL Solution | Randob Ltd. | OTC MONOGRAPH NOT FINAL |
Frequently asked questions
What is Fire Out used for?
Uses ▪ Temporarily relieves pain and itching of fire ant bites and stings, insect bites and stings, and minor skin irritation.
Who makes Fire Out?
Fire Out is listed by 1 labeler in the FDA NDC directory, including Randob Ltd..