FDA Label for Numit
View Indications, Usage & Precautions
Numit 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% BENZOCAINE HYDROCHLORIDE, 2.00% LIDOCAINE HYDROCHLORIDE, 2.00% TETRACAINE HYDROCHLORIDE
Inactive Ingredients
ETHYL ALCOHOL, PROPYLENE GLYCOL, AND TETRASODIUM EDTA
Indications & Usage
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.
Warnings
CLIENT EYE PROTECTANT SUGGESTED
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.
Caution
DISCONTINUE USE IF YOU HAVE SKIN IRRITATION OR SENSITIVITY.
Other
Distributed by
Permanent Make Up Products LLC.
Principal Display Panel - 14 G Bottle Label
NUMIT LIQUID
FOR PROFESSIONAL USE ONLY
1/2 FL OZ. (14G)
PMUP
PERMANENT
MAKE UP PRODUCTS
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