FIRST AID ONLY FIRST AID/BURN- lidocaine hydrochloride, benzalkonium chloride cream 
Acme United Corporation

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First Aid Only First Aid/Burn Cream

Drug Facts

Active Ingredients

Benzalkonium chloride 0.13%

Lidocaine HCL 0.5%

Purpose

First Aid Antiseptic

External Analgesic

Uses

First aid to help prevent infection and for the temporary relief of pain and itching associated with minor: cuts, •scrapes, •burns.

Warnings

For external use only.

Do not use

▪in the eyes ▪over large areas of the body ▪in large quantities, particularly over raw surfaces or blistered areas ▪if you are allergic to any of the ingredients ▪on deep puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

▪condition worsens or clears up and occurs again within a few days ▪symptoms persist for more than 7 days

Keep out of reach of children.

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

Directions

Adults - Clean the affected area, apply a small amount of product (equal to the surface area of a fingertip) 1 to 3 times daily.

Children under 2- Consult a doctor



Other Information

Store at room temperature

Inactive Ingredients

butylated hydroxytoluene, cetostearyl alcohol, dimethicone, edetate sodium, glycerin, glyceryl monostearate, isopropyl myristate, macrogol cetostearyl ether 20, methylcellulose, purified water, sodium methylparaben, sodium propylparaben

Questions

1.800.835.2263

Carton Label Carton Label

FIRST AID ONLY FIRST AID/BURN 
lidocaine hydrochloride, benzalkonium chloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5730(NDC:61040-007)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE5 mg  in 1 g
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
WATER (UNII: 059QF0KO0R)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-5730-000.9 g in 1 PACKET; Type 0: Not a Combination Product10/16/2023
2NDC:0924-5730-0212 in 1 CARTON10/16/2023
20.9 g in 1 PACKET; Type 0: Not a Combination Product
3NDC:0924-5730-0325 in 1 CARTON10/16/2023
30.9 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00310/16/2023
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-5730) , repack(0924-5730)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599repack(0924-5730) , relabel(0924-5730)

Revised: 10/2023
Document Id: 07247305-a6fe-50c3-e063-6294a90a6721
Set id: 07245b54-b193-178e-e063-6394a90a2581
Version: 1
Effective Time: 20231009
 
Acme United Corporation