FDA Label for Magic Plus Anesthetic
View Indications, Usage & Precautions
Magic Plus Anesthetic Product Label
The following document was submitted to the FDA by the labeler of this product Permanent Make Up Products Llc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
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
Otc - Purpose
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. Store in a cool, dark place. Do not refrigerate.
Other
CLIENT EYE PROTECTANT SUGGESTED
Distributed by
Permanent Make Up Products LLC.
Otc - Pregnancy Or Breast Feeding
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
Keep out of the reach of children. If product comes into contact with the eyes wash immediatley. If accidentally swallowed seek immediate medical attention.
Otc - Do Not Use
Do not use this product if you have any allergies to any of the product ingredients.
Otc - Stop Use
CAUTION: DISCONTINUE USE IF YOU HAVE SKIN IRRITATION OR SENSITIVITY.
Principal Display Panel - 28 G Bottle Label
MAGIC
PLUS TOPICAL ANESTHETIC GEL
RELIEVES PAIN & SWELLING
WORKS IN SECONDS
FOR PROFESSIONAL USE ONLY
1 FL OZ. (28G)
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