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First Aid and Burn by Acme United Corporation

Medically reviewed on May 24, 2018

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%

Purpose

First Aid Antiseptic

Topical analgesic

Uses
  • for the temporary relief of pain associated with minor burns
  • helps protect against harmful bacteria

Warnings

For external use only

Keep out of reach of children.

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

Do not use
  • in eyes
  • in large quantities
  • over raw or blistered areas, or on deep puncture wounds, animal bites, serious burns
  • for more than one week unless directed by a doctor

Stop use and ask a doctor if
  • the condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days

Directions

Adults and children 2 years and over: clean affected area, apply small amount not more than 3 to 4 times daily

Children under 2 years: do not use, consult a doctor

Other information
  • store at room temperature (do not freeze)
  • do not use any opened or torn packets

Inactive ingredients

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

Questions?

1-800-275-3433

PRINCIPAL DISPLAY PANEL – Pac-Kit 12 count box

PAC-KIT
FIRST AID

First Aid
Burn Cream
Packets

Paquetes de crema
para quemaduras

12 First Aid Burn
Cream Packets,
0.9gm ea.

12 paquetes,
0,9 gm cada uno.

Reorder #13-006

ANSI Z308. 1-2009

FIRST AID AND BURN 
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 hydrochloride5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
aloe vera leaf 
alcohol 
methylparaben 
mineral oil 
paraffin 
propylparaben 
water 
petrolatum 
white wax 
Packaging
#Item CodePackage Description
1NDC:0924-5701-0512 PACKET (12 PACKET) in 1 BOX
1NDC:0924-5701-010.9 g in 1 PACKET
2NDC:0924-5701-0625 PACKET (25 PACKET) in 1 BOX
2NDC:0924-5701-010.9 g in 1 PACKET
3NDC:0924-5701-0760 PACKET (60 PACKET) in 1 BOX
3NDC:0924-5701-010.9 g in 1 PACKET
4NDC:0924-5701-08144 PACKET (144 PACKET) in 1 BOX
4NDC: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)
Establishment
NameAddressID/FEIOperations
Safetec of America, Inc.874965262MANUFACTURE(0924-5701)

 
Acme United Corporation

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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