FIRST AID ONLY FIRST AID/BURN- lidocaine hydrochloride and 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 ▪a rash or allergic reaction occurs

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 in a cool dry area 150 – 250C (590 – 770F)

INACTIVE INGREDIENTS

butylated hydroxytoluene, ceteth-20, cetostearyl alcohol, dimethicone, glycerin, glyceryl monostearate, isopropyl myristate, methylcellulose, purified water, sodium EDTA, methyl paraben sodium, propylparaben sodium

Questions 1.800.835.2263

carton label Carton Label

FIRST AID ONLY FIRST AID/BURN 
lidocaine hydrochloride and benzalkonium chloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5011(NDC:50382-022)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 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)  
CETETH-20 (UNII: I835H2IHHX)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
METHYLCELLULOSE (25 MPA.S) (UNII: BI55GG2WLI)  
WATER (UNII: 059QF0KO0R)  
EDETATE SODIUM (UNII: MP1J8420LU)  
METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-5011-000.9 g in 1 PACKET; Type 0: Not a Combination Product08/30/2021
2NDC:0924-5011-0212 in 1 CARTON08/30/2021
20.9 g in 1 PACKET; Type 0: Not a Combination Product
3NDC:0924-5011-0325 in 1 CARTON08/30/2021
30.9 g in 1 PACKET; Type 0: Not a Combination Product
4NDC:0924-5011-0110 in 1 CARTON08/30/2021
40.9 g in 1 PACKET; Type 0: Not a Combination Product
5NDC:0924-5011-04144 in 1 CARTON08/30/2021
50.9 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/30/2021
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-5011) , repack(0924-5011)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599relabel(0924-5011) , repack(0924-5011)

Revised: 11/2024
Document Id: 27225914-f582-736b-e063-6394a90ad1c5
Set id: caa67a05-bdbd-c380-e053-2995a90a0bf1
Version: 2
Effective Time: 20241117
 
Acme United Corporation