FIRST AID ONLY STING RELIEF- benzocaine swab

First Aid Only Sting Relief by

Drug Labeling and Warnings

First Aid Only Sting Relief by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzocaine 20 percent

Menthol 1 percent

PURPOSE

Topical Analgesic

Topical Analgesic

INDICATIONS & USAGE

Uses

For temporary relief of the pain and itching of

insect bites and stings

minor scrapes and burns

WARNINGS

Warnings

For external use only.

Do not use

in the eyes if you are allergic to any of the ingredients

Stop use and ask a doctor if conditions worsen symptoms clear up and then recur the condition persists for more than 7 days

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children

If swallowed, contact Poison Control 800.222.1222, or a doctor immediately.

DOSAGE & ADMINISTRATION

Directions If stinger is present, remove carefully if possible.

Adults Reverse cardboard sleeve so swab is visible. With cardboard sleeve on ampile, crush at dot on sleeve.

There will be a "pop" and the swab will become saturated. Apply saturated applicator to the affected area no more than

3 to 4 times daily.

Children under 2 Consult a doctor.

INFORMATION FOR PATIENTS

Other Information

Store at room temperature.

INACTIVE INGREDIENT

D&C Green no. 5, D&C yellow no.10, FD&C blue no.1, isopropyl alcohol, polyethylene glycol 300, purified water

QUESTIONS

Questions 800.835.2263

PRINCIPAL DISPLAY PANEL

BOX19001-revD (002).jpg

INGREDIENTS AND APPEARANCE

FIRST AID ONLY STING RELIEF 
benzocaine swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-5250(NDC:46414-2040)
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	0.12 g  in 0.6 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.006 g  in 0.6 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-5250-01	10 in 1 CARTON	02/01/2010
1		6 mL in 1 AMPULE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/01/2010

Labeler - Acme United Corporation (001180207)

Registrant - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-5250) , repack(0924-5250)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-5250) , repack(0924-5250)