MEDI-FIRST PLUS BURN CREAM- lidocaine cream

Medi-First Plus Burn Cream by

Drug Labeling and Warnings

Medi-First Plus Burn Cream by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium chloride 0.13%

Lidocaine HCl 0.5%

Purpose

Topical antiseptic

Topical analgesic

Uses

Firt aid to help prevent infection in minor cuts, scrapes and burns.

For temporary relief of pain and itching associated with:

• sunburn
• minor burns
• insect bites
• minor skin irritation
• cuts
• scrapes

Warnings

For external use only.

Do not use

• in the eyes
• over large areas of the body or on deep puncture wounds, animal bites or serious burns
• in large quantities, particularly over raw surfaces or blistered areas

Stop use and ask a doctor if

• condition gets worse
• condition clears up and recurs within a few days
• condition persists for more than 7 days

If pregnant or breast feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

Adults and children 12 years and over:

• clean the affected area
• apply a small amount of this product on the area 3 to 4 times daily
• may be covered with a sterile bandage

Children under 12 years:

• consult a doctor

Other information

• store in a cool, dry area
• 59° to 79° F (15° to 25° C)
• tamper evident sealed packets
• do not use any open or torn packets

Inactive ingredients

buttylated hydroxytoluene, cetomacrogol, cetostearyl alcohol, dimethicone, glycerine, glyceryl monostearate, isopropyl myristate, methylcellulose, purified water, sodium EDTA, sodium methylparaben, sodium propylparaben

Questions or comments?

1-800-634-7680

Medi-First Plus Burn Cream Label

Medi-First Plus®

Burn Cream with Lidocaine

25 Units of 0.9gm Packets

Item #93973

INGREDIENTS AND APPEARANCE

MEDI-FIRST PLUS BURN CREAM 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-937
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	0.5 g  in 100 g
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
METHYLCELLULOSE (25 MPA.S) (UNII: BI55GG2WLI)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
DIMETHICONE (UNII: 92RU3N3Y1O)
CETETH-20 (UNII: I835H2IHHX)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-937-73	25 in 1 BOX	04/14/2016
1		0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/01/2015

Labeler - Unifirst First Aid Corporation (832947092)