AFTER BITE WIPE INSECT STING RELIEF- benzocaine,alcohol swab

After Bite Wipe Insect Sting Relief by

Drug Labeling and Warnings

After Bite Wipe Insect Sting Relief by is a Otc medication manufactured, distributed, or labeled by Tender Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzocaine, 6%

SD alcohol, 60%

Purpose

Topical Analgesic
Antiseptic

Use

temporarily relieves pain and itching due to minor stings and insect bites

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

• over large areas of the body
• in the eyes
• on broken skin or deep puncture wounds

Stop use and ask a doctor if

condition worsens or if symptoms persist for more than 7 days or clears up and occurs 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 year of age and older: apply to affected area not more than 3 to 4 times daily.
• children under 2 years of age: consult a doctor

Other information

Store at room temperature

Inactive Ingredient

Purified water

PRINCIPAL DISPLAY PANEL

After Bite Wipe Insect Sting Relief

1 single use wipes

Responsibly made in China for:

Tender Corporation

944 Industrial park Rd.

Littleton, NH

afterbite.com

INGREDIENTS AND APPEARANCE

AFTER BITE WIPE INSECT STING RELIEF 
benzocaine,alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44224-0014
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44224-0014-1	1000 mg in 1 PACKAGE; Type 0: Not a Combination Product	09/01/2019
2	NDC: 44224-0014-2	100 in 1 BOX	09/01/2019
2		1000 mg 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	part333E	09/01/2019

Labeler - Tender Corporation (064437304)