FIRST AID ONLY STING RELIEF PAD- benzocaine, isopropyl alcohol liquid 
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

Drug Facts


Active ingredients

Benzocaine 6.0%

Isopropyl Alcohol 60% w/v

Purpose

Topical Anesthetic

Antiseptic

For the temporary relief of pain and itching associated with minor scrapes and insect bites.

First aid to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only

Flammable, keep away from fire or flame

Do Not Use

  • in eyes, if contact occurs flush with water ▪over large areas of the body

Consult a doctor ▪if condition worsens ▪if symptoms last for more than seven days or clear up and occur again ▪for deep puncture wounds

Keep out of reach of children.

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

Directions

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

▪Children under 2 years: consult physician

Inactive ingredient

Purified Water

Other information store at room temperature

Pouch labelpouch label

FIRST AID ONLY STING RELIEF PAD 
benzocaine, isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5204(NDC:59050-414)
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 ALCOHOL600 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-5204-05100 in 1 BOX02/25/2022
10.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC:0924-5204-0450 in 1 BOX02/25/2022
20.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3NDC:0924-5204-0325 in 1 BOX02/25/2022
30.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
4NDC:0924-5204-0210 in 1 BOX02/25/2022
40.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
5NDC:0924-5204-010.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)02/25/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/25/2022
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-5204) , repack(0924-5204)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599relabel(0924-5204) , repack(0924-5204)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation117825595manufacture(0924-5204)

Revised: 2/2022
Document Id: d71047f6-1354-c758-e053-2995a90a962c
Set id: d71047f6-1353-c758-e053-2995a90a962c
Version: 1
Effective Time: 20220203
 
Acme United Corporation