SOOTH-A-STING- benzocaine, isopropyl alcohol swab

Sooth-a-Sting by

Drug Labeling and Warnings

Sooth-a-Sting by is a Otc medication manufactured, distributed, or labeled by HART Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzocaine 6%

Isopropyl Alcohol 60%

Purpose

Topical Anesthetic

Topical Antiseptic

Uses

Temporarily relief of pain and itching associated with

• insect bites
• insect stings

Warnings

For external use only

do not get in eyes

not for prolonged use

FLAMMABLE keep away from heat and flame

Allergy alert: A severe allertic reaction to insect bites and stings may require life support measures. In such cases, immediately call 911 or your local emergency provider.

Do not use

• more than 3 to 4 times daily
• in or near the eyes or over large portions of the body

Stop use and ask a doctor if

• symptoms last more than 3 days
• unusual redness, swelling, rash, or other irriation occurs

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away 1-800-222-1222

Directions

Adults and chldren 2 years of age and older:

• remover stinger carefully
• gently wipe on and around point of insect puncture
• do not reuse wipe
• dispose of wipe properly

Children under 2 years of age:

• ask a doctor

Inactive Ingredient

Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOOTH-A-STING 
benzocaine, isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50332-0048
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	.06 g  in 1 g
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	.60   in 1 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50332-0048-1	10 in 1 BOX	04/01/1974
1		.35 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 50332-0048-7	100 in 1 PACKAGE	04/20/2016
2		.35 g 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	04/01/1974

Labeler - HART Health (069560969)