NEKVNRO DENTAL VENEERS- dental veneers patch

Nekvnro Dental Veneers by

Drug Labeling and Warnings

Nekvnro Dental Veneers by is a Otc medication manufactured, distributed, or labeled by Guoyu Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Menthol 0.5%

Purpose

Relieve tooth pain

Use

Keep hands dry and take off the strips

Gently press it onto the teeth

Leave the patch on for 30 minutes，Do not eat or drink during the process

Remove and discard the patch，Then rinse off the excess gel.

Warnings

Avoid contact with eyes and skin

Do not use

Should not be used if you have mouth sores/exposed gums or after oral surgery

When Using

Disposable products Please do not reuse,Not for use by children under 16 years old

Stop Use

If you experience any discomfort, stop using and consult a dentist immediately

Ask Doctor

If you experience any discomfort, stop using and consult a dentist immediately

Keep Oot Of Reach Of Children

Not for use by children under 16 years old，keep out of reach of children.

Directions

Keep hands dry and take off the strips

Gently press it onto the teeth

Leave the patch on for 30 minutes，Do not eat or drink during the process

Remove and discard the patch，Then rinse off the excess gel.Please store in a dry and cool place away from direct sunlight ,keep out of reach of young children.

Other information

To achieve and maintain better results，Minimize or avoid smoking、Drink coffee、Tea、Coke or red wine，And edible cherries，blueberry，Highly pigmented foods

Inactive ingredients

Glycerol，Propylene Glycol，Water，Sodium Phytate，Carbomer，Carboxymethyl，Polyvinylpyrrolidone，Sodium Hydroxide

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO DENTAL VENEERS 
dental veneers patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	0.5 g  in 100

Inactive Ingredients
Ingredient Name	Strength
CARBOMER (UNII: 0A5MM307FC)
CARBOXYMETHYLCELLULOSE CALCIUM (UNII: UTY7PDF93L)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYVINYL ALCOHOL (94000 MW) (UNII: C1MS7RRZ6L)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
SODIUM PHYTATE (UNII: 88496G1ERL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-006-01	28 in 1 BOX; Type 0: Not a Combination Product	10/31/2024
2	NDC: 84844-006-02	48 in 1 BOX; Type 0: Not a Combination Product	10/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/31/2024

Labeler - Guoyu Trading Co., Ltd. (963348600)

Establishment
Name	Address	ID/FEI	Business Operations
Guoyu Trading Co., Ltd.		963348600	manufacture(84844-006)