Active Ingredient
Propylene Glycol
Professional Level Brighting Pen
FDA Label NDC 84732-087
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongguan Haiyi Technology Co.,ltd. for the product Professional Level Brighting Pen (NDC 84732-087). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, inactive ingredient, purpose section, warning, stop use, not use, out of children, how to use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Aqua, Glycerin,Carbomer, Cellulose Gum, EDTA,Menthol, PVP, Sodium Bicarbonate,Sodium Chlorite.
Purpose Section
Tooth Brighting
Warning
For cosmetic use only.
Do not swallow. Avoid contact with eyes.
Store in a cool area away from heat.
Keep out of reach of children.
Stop Use
This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.
Not Use
Not suitable for use by children, pregnantor breast feeding people.
Out Of Children
KEEP THE PRODUCT OUT OF REACH OF CHILDREN to
How To Use
Step 1:Brush your teeth.
Step 2:Twist the base of the pen until you see gel.
Step 3:Apply the gel in a brushing motion.
Step 4:Rinse mouth after 1 minute.
Dosage
Once a day in the morning and evening
Package Label.Principal Display Panel
Label (C597810157e44ffdafe549c2bc6316ff)
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