PROFESSIONAL LEVEL BRIGHTING PEN liquid

Professional Level Brighting Pen by

Drug Labeling and Warnings

Professional Level Brighting Pen by is a Otc medication manufactured, distributed, or labeled by Dongguan Haiyi Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Propylene Glycol

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROFESSIONAL LEVEL BRIGHTING PEN 
professional level brighting pen liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-087
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPROPYLENE GLYCOL (UNII: E107L85C40) (DIPROPYLENE GLYCOL - UNII:E107L85C40)	DIPROPYLENE GLYCOL	1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MENTHOL (UNII: L7T10EIP3A)
PVP (UNII: FZ989GH94E)
SODIUM CHLORITE (UNII: G538EBV4VF)
WATER (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
EDTA (UNII: 9G34HU7RV0)
CELLULOSE GUM (UNII: K679OBS311)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-087-01	2 mL in 1 TUBE; Type 0: Not a Combination Product	11/06/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	11/06/2024

Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-087)