BITE AND STING RELIEF WIPE- alcohol 50% lidocaine hcl 2% cloth

Bite and Sting Relief Wipe by

Drug Labeling and Warnings

Bite and Sting Relief Wipe by is a Otc medication manufactured, distributed, or labeled by CVS, Diamond Wipes International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 50.0%

Lidocaine HCL 2.0%

Purpose

First Aid Antiseptic
Topical Analgesic

Uses

• First aid to help guard against skin infection and temporary relief of pain and itching assocaiated with insect bites.

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

• in the eyes over large areas of the body or bandage. 
• in large quantities particularly over raw surfaces or blistered areas.

Stop use and contact a doctor if the condition persists or worsens for more than 7 days or clears up and occurs again within a few days.

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

Adults and children 2 years and older: Apply to clean affected area no more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Inactive ingredients

Benzalkonium Chloride, Menthol, Water.

Packaging

INGREDIENTS AND APPEARANCE

BITE AND STING RELIEF WIPE 
alcohol 50% lidocaine hcl 2% cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-190
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	50 mL  in 100 mL
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	white	Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-190-10	30 in 1 BOX	06/01/2019
1		3 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/01/2019

Labeler - CVS (062312574)

Establishment
Name	Address	ID/FEI	Business Operations
Diamond Wipes International, Inc.		161104729	manufacture(69842-190)