FIRST AID BURN CREAM cream

First Aid Burn Cream by

Drug Labeling and Warnings

First Aid Burn Cream by is a Otc medication manufactured, distributed, or labeled by Front Line Safety. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine Hydrochloride 0.5%

Purpose

Topical Analgestic

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Topical Antiseptic

Use(s)

For the temporary relief of pain and itching associated with:

Sunburn Minor burns Insect bites Minor skin irritations 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 aks a doctor if

The condition get 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 care prfessional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Adults and children 2 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 2 years: Consult a doctor

Other Information

Store in a cool, dry area 15º-25ºC (59º-77ºF)

Tamper evident sealed packets

Do not use any opened or torn packets

Inactive Ingredients

Butylated Hydroxytoluene, Cetomacrogol 1000, Cetostearyl Alcohol, Dimethicone, Glycerine, Glyceryl Monostearate, Isopropyl Myristate, Methylcellulose, Purified Water, Sodium EDTA, Sodium Methylparaben, Sodium Propylparaben

Questions?

1-888-900-2920 Monday - Friday 8AM-4PM PST

Label

FL-2044

INGREDIENTS AND APPEARANCE

FIRST AID BURN CREAM 
first aid burn cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58228-6244
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	50 mg  in 10000 mg
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	13 mg  in 10000 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
CETETH-20 (UNII: I835H2IHHX)
METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
WATER (UNII: 059QF0KO0R)
EDETATE SODIUM (UNII: MP1J8420LU)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
METHYLCELLULOSE (4000 MPA.S) (UNII: MRJ667KA5E)
DIMETHICONE 350 (UNII: 2Y53S6ATLU)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58228-6244-1	1800 in 1 CASE	01/26/2024
1		25 in 1 BOX
1		900 mg 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 Drug	M017	01/26/2024

Labeler - Front Line Safety (061263699)