Magic Plus Topical Anesthetic Spray

Manufacturer
Tri-Lab Products Inc.
Effective date
2024-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:06:55

Label at a glance#

ProductMagic Plus Anesthetic
Active ingredientLidocaine Hydrochloride, Tetracaine Hydrochloride, Racepinephrine Hydrochloride
Label structure7 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

FOR EXTERNAL USE ONLY

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

For temporary relief of pain and swelling.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

WARNINGS

WARNINGS SECTION

CLIENT EYE PROTECTANT SUGGESTED

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - DO NOT USE SECTION

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

CAUTION

OTC - STOP USE SECTION

DISCONTINUE USE IF YOU HAVE SKIN IRRITATION OR SENSITIVITY.

SPL UNCLASSIFIED SECTION

Distributed by Trilab Products Inc. 714.839.6543.

PRINCIPAL DISPLAY PANEL - 28 G Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Original!
Magic
Plus

TOPICAL ANESTHETIC SPRAY
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
PRINCIPAL DISPLAY PANEL - 28 G Bottle Label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84112-00884112-008-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
167b9e84-727a-4cde-a32c-d2b5003d036da50b14f8-114d-49cd-a596-08d167cbe89b2024-07-11WarningsExact identifier
spl set id: a50b14f8-114d-49cd-a596-08d167cbe89b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.