BE SMART GET PREPARED STING RELIEF WIPE- alcohol, lidocaine hydrochloride liquid

Be Smart Get Prepared Sting Relief Wipe by

Drug Labeling and Warnings

Be Smart Get Prepared Sting Relief Wipe by is a Otc medication manufactured, distributed, or labeled by Total Resources International, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl alcohol 56.6% v/v

Lidocaine HCl 2.0% w/w

Purpose

First Aid Antiseptic

Topical Analgesic

Uses

First aid to help prevent infection in minor scrapes and temporary relief of itching of insect bites

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

• over large areas of the body
• in eyes
• over raw or blistered areas

Stop use and ask doctor if conditions worsen or persist for more than 7 days or clear up and occur again within a few days.

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 cleaned affected area not more than 3 times daily. Children under 2 years of age: Consult a doctor.

Inactive ingredients

benzalkonium chloride, menthol, purified water

Principal Display Panel – 0.8 g Pouch Label

BE SMART®

GET PREPARED

STING RELIEF
WIPE

DO NOT FLUSH

SINGLE USE

Temporary Relief from Stings & Bites

Made in USA Manufactured forTotal Resources Inti. Inc.

Walnut, California 91789 www.besmartgetprepared.com

00-BEE-90103 Rev.03 NDC: 55550-201 -03

1PC

INGREDIENTS AND APPEARANCE

BE SMART GET PREPARED STING RELIEF WIPE 
alcohol, lidocaine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55550-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	0.566 mL  in 1 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	Lidocaine Hydrochloride Anhydrous	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
benzalkonium chloride (UNII: F5UM2KM3W7)
menthol (UNII: L7T10EIP3A)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55550-201-03	1 mL in 1 PACKET; Type 0: Not a Combination Product	05/20/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	05/20/2022

Labeler - Total Resources International, Inc (790160535)