FIRST AID ONLY STING RELIEF PAD- benzocaine swab 
Acme United Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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First Aid Only Sting Relief Pad

Active Ingredients

Benzocaine, 6% w/v

Isopropyl Alcohol 60% w/v

Purpose

Topical Anesthetic

Antiseptic

Use

For the temporary relief of pait and itching associated with minor burns, scrapes and insect bites. First aid to help prevent infection in minor cuts, scrapes, and burns

Directions

▪adults and children 2 years of age or older, apply to affected area not more than 3 to 4 times daily

▪children under 2 years: consult a physician

Warnings

For external use only

Flammable, keep away from fire or flames

Do not use

  • In the eyes. If contact occurs, rinse thoroughly with water
  • over large areas of the body

Stop use

If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Keep out of reach of children.

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

Inactive Ingredients

Purified Water

Other Information

Store at room temperature

Principal Display Panel - 0.4 mL Pouch Label

0.4 mL Pouch Label 0.4 mL Pouch Label

FIRST AID ONLY STING RELIEF PAD 
benzocaine swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5203(NDC:65517-0005)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE60 mg  in 1 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.6 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-5203-010.4 mL in 1 POUCH; Type 0: Not a Combination Product04/08/2019
2NDC:0924-5203-0210 in 1 BOX04/08/2019
20.4 mL in 1 POUCH; Type 0: Not a Combination Product
3NDC:0924-5203-0325 in 1 BOX04/08/2019
3NDC:0924-5203-010.4 mL in 1 POUCH; Type 0: Not a Combination Product
4NDC:0924-5203-04100 in 1 BOX04/08/2019
4NDC:0924-5203-010.4 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/08/2019
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-5203) , repack(0924-5203)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599relabel(0924-5203) , repack(0924-5203)

Revised: 4/2019
Document Id: 85dec352-6cad-03fa-e053-2a91aa0a8715
Set id: 85dec352-6cac-03fa-e053-2a91aa0a8715
Version: 1
Effective Time: 20190406
 
Acme United Corporation