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First Aid and Burn by Acme United Corporation

Dosage form: cream
Ingredients: benzalkonium chloride 1.3mg in 1g, lidocaine hydrochloride 5mg in 1g
Labeler: Acme United Corporation
NDC Code: 0924-5701

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.

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Lidocaine HCl 0.5%


First Aid Antiseptic

External analgesic


first aid to help prevent infection and for the temporary relief of itching associated with

  • minor cuts
  • scrapes
  • burns


For external use only

Do not use
  • in the eyes or apply over large areas of the body
  • longer than 1 week unless directed by a doctor
  • in large quantities, particularly over raw surfaces or blistered areas

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns

When using this product avoid contact with eyes

Stop use and ask a doctor if
  • condition worsens or persists for more than 7 days
  • clears up and occurs again within a few days

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

  • adults and children 2 years of age and older:
  • clean the affected area
  • apply a small amount of this product to the area 1 to 3 times daily
  • may be covered with a sterile bandage
  • children under 2 years of age: consult a doctor

Other information
  • store at room temperature
  • do not use if packet is opened or torn

Inactive ingredients

aloe vera, emulsifying wax, ethyl alcohol, methylparaben, mineral oil, paraffin, propylparaben, purified water, white petrolatum, white wax

Questions? 1-800-835-2263

1 800 835 2263

Principal Display Panel - Packet Label


Burn Cream

NET WT 1/32 oz (0.9g)

© 2015 Acme United Corporation.

Faifield, CT 06824


NDC 0924-5701-01

Principal Display Panel - Packet Label




First Aid/Burn Cream

12 (0.9g) Packets

Ungüento de primeros auxilios/para quemaduras

12 sobres de (0.9g)

NDC 0924-5701-10

benzalkonium chloride, lidocaine hydrochloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5701
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
benzalkonium chloride (benzalkonium) benzalkonium chloride1.3 mg  in 1 g
lidocaine hydrochloride (lidocaine) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
aloe vera leaf 
mineral oil 
white wax 
#Item CodePackage Description
1NDC:0924-5701-0410 PACKET in 1 BOX
1NDC:0924-5701-010.9 g in 1 PACKET
2NDC:0924-5701-0910 PACKET in 1 BOX
2NDC:0924-5701-010.9 g in 1 PACKET
3NDC:0924-5701-1012 PACKET in 1 BOX
3NDC:0924-5701-010.9 g in 1 PACKET
4NDC:0924-5701-1125 PACKET in 1 BOX
4NDC:0924-5701-010.9 g in 1 PACKET
5NDC:0924-5701-12144 PACKET in 1 BOX
5NDC:0924-5701-010.9 g in 1 PACKET
6NDC:0924-5701-1360 PACKET in 1 BOX
6NDC:0924-5701-010.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/27/2012
Labeler - Acme United Corporation (001180207)
Registrant - Safetec of America, Inc. (874965262)
Safetec of America, Inc.874965262MANUFACTURE(0924-5701)

Revised: 03/2016
Acme United Corporation

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.