FIRST AID DIRECT SOOTHE-A-STING- benzocaine swab sponge

First Aid Direct Soothe-A-Sting by

Drug Labeling and Warnings

First Aid Direct Soothe-A-Sting by is a Otc medication manufactured, distributed, or labeled by Cintas Corporation, JAMES ALEXANDER CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients (each swab)

Benzocaine (20%), L-Methanol (1%)

PURPOSE

Purpose

Analgesic

Uses

For the temporary relief of pain and itching associated with insect bites and stings

Warnings

FOR EXTERNAL USE ONLY

• do not use in the eyes

• not for prolonged use

Stop use and ask doctor

if condition for this preparation is used persists, or if a rash or irritation develops.

Keep out of reach of children. 

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

Reverse cardboard sleeve then crush at dot between thumb and forefinger. Once solution has saturated tip, apply to sting or bite.

Other Information

Store at room temperature away from light.

Inactive Ingredients

D&C Green Dye #5, D&C Yellow Dye #10, FD&C Blue Dye #1, PEG 300 NF, Isopropyl Alcohol, Purified Water, USP

Questions? 

Call 1-908-362-9266 Monday through Friday, 9:00am - 5:00pm e.s.t

Principal Display Panel - Box

10 SWABS

(1/2 ml.)

UNIT NO

U1-19

SOOTHE-A-STING-SWABS

(FOR INSECT STINGS)

ACTIVE INGREDIENTS: 

BENZOCAINE 20%

MENTHOL 1%

DISTRIBUTED BY

first aid direct®

Mason, OH 45040

INGREDIENTS AND APPEARANCE

FIRST AID DIRECT SOOTHE-A-STING 
benzocaine swab sponge

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42961-107
Route of Administration	topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	20 mg  in 100 mg
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	1 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42961-107-02	10 in 1 BOX	05/16/2022
1		0.5 mg in 1 AMPULE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/16/2022

Labeler - Cintas Corporation (056481716)

Establishment
Name	Address	ID/FEI	Business Operations
JAMES ALEXANDER CORP		040756421	manufacture(42961-107)