ACTIVE INGREDIENTS

5.00% LIDOCAINE HYDROCHLORIDE, 2.00% TETRACAINE HYDROCHLORIDE, 0.02% RACEPINEPHRINE HYDROCHLORIDE

INACTIVE INGREDIENTS

DEIONIZED WATER, HYDROXYETHYL CELLULOSE, SODIUM METABISULFITE, SODIUM CHLORIDE, PROPYLENE GLYCOL, METHYLPARABEN, PROPYLPARABEN, DIAZOLIDINYL UREA, AND TETRASODIUM EDTA

FOR EXTERNAL USE ONLY

For temporary relief of pain and swelling.

DIRECTIONS

Sensitivity test is strongly advised prior to use. Apply to area for temporary relief. Do not use more than 2 times a day.

WARNINGS

CLIENT EYE PROTECTANT SUGGESTED

Do not get in the mouth or eyes. Do not use product if you are pregnant or a nursing mother.

Keep out of the reach of children. If product comes into contact with the eyes wash immediately. If accidentally swallowed seek immediate medical attention.

Do not use this product if you have any allergies to any of the product ingredients.

CAUTION

DISCONTINUE USE IF YOU HAVE SKIN IRRITATION OR SENSITIVITY.

Distributed by Trilab Products Inc.

PRINCIPAL DISPLAY PANEL - 28 G Bottle Label

Original!
Magic
Plus

TOPICAL ANESTHETIC GEL
Magic Works In Seconds!

RELIEVES PAIN
& SWELLING

1 FL OZ. (28 G)

FOR PROFESSIONAL USE ONLY

Store in a cool, dark place - Do not refrigerate!

PRINCIPAL DISPLAY PANEL - 28 G Bottle Label

MAGIC PLUS ANESTHETIC
lidocaine hydrochloride, tetracaine hydrochloride, and racepinephrine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:84112-007
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Lidocaine Hydrochloride (UNII: V13007Z41A) (Lidocaine - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	50 g in 1000 g
Tetracaine Hydrochloride (UNII: 5NF5D4OPCI) (Tetracaine - UNII:0619F35CGV)	Tetracaine Hydrochloride	20 g in 1000 g
Racepinephrine Hydrochloride (UNII: 336096P2WE) (Racepinephrine - UNII:GR0L9S3J0F)	Racepinephrine	200 mg in 1000 g

Ingredient Name	Strength
Inactive Ingredients
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
Sodium Chloride (UNII: 451W47IQ8X)
Water (UNII: 059QF0KO0R)
Propylene Glycol (UNII: 6DC9Q167V3)
Propylparaben (UNII: Z8IX2SC1OH)
Methylparaben (UNII: A2I8C7HI9T)
Diazolidinyl Urea (UNII: H5RIZ3MPW4)
HYDROXYETHYL CELLULOSE (280 MPA.S AT 2%) (UNII: 12VCE9HR9E)
EDETATE SODIUM (UNII: MP1J8420LU)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:84112-007-01	1 in 1 BOX	04/01/2024
1		28 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph drug	M017	04/01/2024

Labeler - Tri-Lab Products Inc. (032851956)