BURN WITH LIDOCAINE- benzalkonium chloride, lidocaine hydrochloride cream
Unifirst First Aid Corporation

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.

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Medi-First Burn Cream with Lidocaine

Drug Facts

Active ingredients

Benzalkonium Chloride 0.13%

Lidocaine HCl 0.5%

Purpose

First aid antiseptic

Topicall analgesic

Uses

for the temporary releif of pain associated with minor burns
helps protect against harmful bacteria

Warnings

For external use only.

Do not use

in the eyes
in large quantities
over raw surfaces or blistered areas, or on deep puncture wounds, animal bites, or serious burns
for more than 1 week unless directed by a doctor

Stop use and ask doctor if

the condition worsens or if symptoms persists for more than 7 days or clear up andoccur again within a few days

Keep out of reach of children.

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

Directions

Adults and children 2 years and over:

clean the affected area, apply a small amount not more than 3 to 4 times daily

Children under 12 years:

do not use, consult a doctor

Other information

store at room temperature (do not freeze)
tamper evident sealed packets
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 or comments? 1-800-634-7680

MF Burn Cream with Lidocaine Label

MEDI-FIRST®

BURN CREAM with Lidocaine

Benzalkonium Chloride 0.13% / Topical Antiseptic

Lidocaine HCl 0.5% / Topical Analgesic

Antiseptic and pain relieving cream for minor cuts, scrapes and burns

Product # 26073

0.9 gram Packets - 25 per box

26073 Burn

BURN WITH LIDOCAINE
benzalkonium chloride, lidocaine hydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-260
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
MINERAL OIL (UNII: T5L8T28FGP)
ALCOHOL (UNII: 3K9958V90M)
METHYLPARABEN (UNII: A2I8C7HI9T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PARAFFIN (UNII: I9O0E3H2ZE)
PETROLATUM (UNII: 4T6H12BN9U)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
WHITE WAX (UNII: 7G1J5DA97F)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-260-73	25 in 1 BOX	01/24/2012
1	NDC:47682-260-99	0.9 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-260-12	10 in 1 BOX	07/03/2017
2		0.9 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-260-99	0.9 g in 1 PACKET; Type 0: Not a Combination Product	01/24/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	01/24/2012

Labeler - Unifirst First Aid Corporation (832947092)

Revised: 10/2022

Document Id: ec1bf303-2bef-6cc9-e053-2a95a90aba9d

Set id: 81363387-d4b1-4c3f-b67f-5017361c0fcd

Version: 13

Effective Time: 20221028

Unifirst First Aid Corporation