MEDI-FIRST PLUS BURN WITH LIDOCAINE- benzalkonium chloride, lidocaine cream 
MEDI-FIRST BURN WITH LIDOCAINE- benzalkonium chloride, lidocaine cream 
Unifirst First Aid Corporation

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Medi-First Burn Cream with Lidocaine

Drug Facts

Active ingredients

Benzalkonium chloride 0.13%

Lidocaine HCl 0.5%

Purposes

First aid antiseptic

External analgesic

Uses

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

Warnings

For external use only.

Do not use

Ask a doctor before use if you have

deep or puncture wounds, animal bites or serious burns

When using this product avoid contact with the eyes

Stop use and ask a doctor if

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

Directions

Other information

Inactive ingredients

aloe barbadensis leaf juice, cetyl alcohol, diazolidinyl urea, disodiun EDTA,, glycerin, glyceryl stearate SE, methylparaben, mineral oil, PEG 100, propylene glycol, propylparaben, stearic acid, triethanolamine, water

Questions or comments? 1-800-634-7680

Medi-First®

Burn Cream with Lidocaine

Benzalkonium Chloride 0.13% / First Aid Antiseptic

Lidocaine HCl 0.5% / External Analgesic

Product # 20669

10 Units Net Wt 0.9 g (1/32 oz)

20669

Medi-First® Plus

Burn Cream with Lidocaine

Benzalkonium Chloride 0.13% / First Aid Antiseptic

Lidocaine HCl 0.5% / External Analgesic

25 Units of 0.9 g Packets

Item #93973

93973

MEDI-FIRST PLUS BURN WITH LIDOCAINE 
benzalkonium chloride, lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-930
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
TROLAMINE (UNII: 9O3K93S3TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
MINERAL OIL (UNII: T5L8T28FGP)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-930-7325 in 1 BOX03/11/202104/30/2028
10.9 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00303/11/202104/30/2028
MEDI-FIRST BURN WITH LIDOCAINE 
benzalkonium chloride, lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-270
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)  
TROLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MINERAL OIL (UNII: T5L8T28FGP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-270-7325 in 1 BOX06/01/202104/30/2028
10.9 g in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-270-1210 in 1 BOX06/01/202104/30/2028
20.9 g in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-270-990.9 g in 1 PACKET; Type 0: Not a Combination Product06/01/202104/30/2028
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00306/01/202104/30/2028
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 1/2024
Document Id: 0f26e626-4d6b-dfdf-e063-6294a90a4c99
Set id: bd46efc8-0b36-0931-e053-2a95a90adb6f
Version: 6
Effective Time: 20240117
 
Unifirst First Aid Corporation