EVERLIGHT SURVIVAL STING RELIEF PAD- benzocaine solution

Everlight Survival Sting Relief Pad by

Drug Labeling and Warnings

Everlight Survival Sting Relief Pad by is a Otc medication manufactured, distributed, or labeled by Yiwu Ori-Power Medtech Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzocaine 6% w/v

SD Alcohol: 60% w/v

Purpose

Topical Anesthetic

Antiseptic

INDICATIONS & USAGE

Uses: For temporary relief of pain and itching associated with minor burns, scrapes, and insect bites

WARNINGS

Warnings:

For external use only

Do not use: In the eyes, on broken skin, deep puncture wounds. If unusal redness, swelling, irritation, or other symptoms occur, consult a physician immediately. 

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

Flammable. Keep away from fire or flame. Avoid contact with eyes. If this happens, rinse thoroughly with water.

Directions

Adults and children 2 yeas of Age or older: Apply to affected area no more than 3-4 times daily

Children under 2 yeas of Age or older: Consult a doctor

INACTIVE INGREDIENT

Inactive Ingredient

Purified Water

Everlight Survival Sting Relief Pad

INGREDIENTS AND APPEARANCE

EVERLIGHT SURVIVAL STING RELIEF PAD 
benzocaine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72459-022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	6 g  in 100 g
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72459-022-01	0.8 g in 1 PATCH; Type 0: Not a Combination Product	06/02/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/02/2025

Labeler - Yiwu Ori-Power Medtech Co.,Ltd. (560451976)