LIGHTS INSTANT STING RELIEF PAD- benzocaine solution

LIGHTS Instant Sting Relief Pad by

Drug Labeling and Warnings

LIGHTS Instant Sting Relief Pad by is a Otc medication manufactured, distributed, or labeled by Lights Medical Manufacture Co., Ltd., Lights Medical Manufacture 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, sunburns, minor cut, scrapes, insect bites, or minor skin irritations

WARNINGS

Warnings:

For external use only. Flammable, keep away from fire or flame. Avoid contact with eyes, if this happens, rinse throughly with water. DO NOT USE with electrocautery procedures.

STOP USE

Stop use and ask a doctor if

• irritation or redness develops
• if condition worsens or persists for more than 7 days, or clear up and occur again within a few days, consult a physician

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

For adults and children 2 yeas of age or older: Apply to affected area not more than 3-4 times daily

Children under 2 yeas of age: Consult a doctor before use

Other Information

Store at room temperature 15-30 C (59-86F). Avoid excessive heat.

INACTIVE INGREDIENT

Inactive Ingredient

Purified Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIGHTS INSTANT STING RELIEF PAD 
benzocaine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61333-214
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: 61333-214-01	100 in 1 BOX	09/03/2024
1		0.8 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/03/2024

Labeler - Lights Medical Manufacture Co., Ltd. (529128649)

Registrant - Lights Medical Manufacture Co., Ltd. (529128649)

Establishment
Name	Address	ID/FEI	Business Operations
Lights Medical Manufacture Co., Ltd.		529128649	manufacture(61333-214)