INSECT BITE RELIEF- benzocaine solution

Insect Bite Relief by

Drug Labeling and Warnings

Insect Bite Relief by is a Otc medication manufactured, distributed, or labeled by Swabplus Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Fact

Active ingredient

Benzocaine 15%

Purpose

Benzocaine for  Pain Relief

Uses

temporary relief of pain and itching associated with insect bites, scrapes, minor cuts, minor burns, sunburn, or skin irritation

Warnings

For external use only. do not bandage.

Do not use. in the eyes or apply over large areas of the body, particularly over raw surfaces or blistered area - if product gets into the eyes. flush throughly with water and obtain medical attention. longer than one week unless directed by doctor.

Stop use and ask a doctor if. condition worsens or if symptoms 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

♦   Do not use if label seal is broken prior to purchase. Keep swabs in original container when not in use.

♦   Hold the swab vertically, with the color band tip upwards. hold in the center of the stem with one hand and at the color band with the other.

♦  Bend the tip at the color band to one side until it snaps.

♦  Apply the product to the affected area.

♦  Discard swab after use.

Administration

For adult and children 2 and older. Apply directly onto affected area no more than 3 to 4 times daily.

Children under 2 years of age. Do not use, consult a doctor.

Other information

Avoid storing at excessive heat.

Inactive ingredients

Aloe Vera Gel. Ethoxydiglycol (diethylene glycol monoethyl ether), Glycerin, Menthol, PEG-8 (Polyethylene glycol 400), Propylene Glycol, Triclosan

Package Display Panel

Image of insect bite carton label

INGREDIENTS AND APPEARANCE

INSECT BITE RELIEF 
benzocaine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65734-300
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzocaine (UNII: U3RSY48JW5) (Benzocaine - UNII:U3RSY48JW5)	Benzocaine	150 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Polyethylene Glycol 400 (UNII: B697894SGQ)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
Glycerin (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
Triclosan (UNII: 4NM5039Y5X)
Menthol (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65734-300-36	36 in 1 PACKAGE
1	NDC: 65734-300-00	0.15 mL in 1 APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	03/01/2003

Labeler - Swabplus Inc. (876441549)

Registrant - Swabplus Inc. (876441549)

Establishment
Name	Address	ID/FEI	Business Operations
Swabplus Inc.		876441549	manufacture(65734-300) , relabel(65734-300) , repack(65734-300)