MEDI-FIRST BURN- lidocaine hcl spray

Medi-First Burn by

Drug Labeling and Warnings

Medi-First Burn 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

Active ingredient

Lidocaine HCl 2.0%

PURPOSE

Purpose

Topical pain relief

INDICATIONS & USAGE

Uses

Temporary pain relief associated with minor burns

WARNINGS

Warnings

For external use only.

DO NOT USE

Do not use

• in large quantities, particularly over raw or blistered areas
• near eyes, if this happens rinse thoroughly with water

STOP USE

Stop use and ask doctor if

condition worsens or persists for more than 7 days or clears up and returns.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Directions

• spray an even layer of burn spray over cleaned affected area not more than 3-4 times daily
• not to be used on children under 12 years of age

INACTIVE INGREDIENT

Inactive ingredients

glycerin, hydroxypropyl methylcellulose, melaleuca alterniflia (tea tree) leaf oil, octoxynol 9, PEG-40 hydronated castor oil, phenoxyethanol, propylene glycol, triethanolamine, water

QUESTIONS

Questions or comments? 1-800-634-7680

Medi-First Burn Spray Label

Medi-First°

Burn Spray

Pump Spray

Lidocaine HCl 2.0%

Topical Analgesic

Relieves pain in minor burns

Store at 68°-77°F (20°-25°C)

2 FL OZ (59.1 ML)

INGREDIENTS AND APPEARANCE

MEDI-FIRST BURN 
lidocaine hcl spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-255
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	20 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
OCTOXYNOL 9 (UNII: 7JPC6Y25QS)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
HYPROMELLOSES (UNII: 3NXW29V3WO)
GLYCERIN (UNII: PDC6A3C0OX)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-255-02	0.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M015	03/01/2021

Labeler - Unifirst First Aid Corporation (832947092)