FIRST AID ONLY STING RELIEF- benzocaine swab 
Acme United Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

First Aid Only Sting Relief Swabs

Benzocaine 20 percent

Menthol 1 percent

Topical Analgesic

Topical Analgesic

Uses

For temporary relief of the pain and itching of

•insect bites and stings

•minor scrapes and burns

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 the reach of children

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

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.

Other Information

Store at room temperature.

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

Questions 800.835.2263

Sting Swabs Carton ImageBOX19001-revD (002).jpg

FIRST AID ONLY STING RELIEF 
benzocaine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5250(NDC:46414-2040)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.12 g  in 0.6 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.006 g  in 0.6 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-5250-0110 in 1 CARTON02/01/2010
16 mL in 1 AMPULE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/01/2010
Labeler - Acme United Corporation (001180207)
Registrant - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-5250) , repack(0924-5250)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599relabel(0924-5250) , repack(0924-5250)

Revised: 4/2018
Document Id: 697127d1-c02f-16d2-e053-2a91aa0a39fd
Set id: 697127d1-c02e-16d2-e053-2a91aa0a39fd
Version: 1
Effective Time: 20180410
 
Acme United Corporation