WHITENING AND ANTI-FRECKLE ESSENCE liquid

Whitening and anti-freckle essence by

Drug Labeling and Warnings

Whitening and anti-freckle essence by is a Otc medication manufactured, distributed, or labeled by Shenzhen Zhumeng Times Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

NIACINAMIDE 3%...... Whitening treatment

Purpose

to Whitening the skin, and nurture the skin barrier.

Uses

Skin regimen is key. Most effective when applied correctly, faithfully, and consistent. Apply a small amount as a thin layer on the affected area twice daily.

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children.lf swallowed, get medical help or contact a Poison Control Center right away.

Dosage and administration

For external use only.

Do not use

Stop use and ask a doctor if

When using section

When using this product keep out of eyes. Rinse with water to remove.

Keep out of reach of children.

If sxralowed, get medical help or contact a Poison Conirol Cenler ngiht away.

Inactive ingredients

AQUA,PROPYLENE GLYCOL,ASCORBIC ACID,NIACINAMIDE,CETEARYL ALCOHOL,ETHYLHEXYL PALMITATE,CETEARYL ALCOHOL,CETEARYL GLUCOSIDE,ERYTHRITOL,GLYCERYL STEARATE,PEG-100 STEARATE,CYCLOPENTASILOXANE,CYCLOHEXASILOXANE,DIMETHICONE,PENTYLENE GLYCOL,CAPRYLHYDROXAMIC ACID,GLYCERYL CAPRYLATE,CARBOMER,METHYLPARABEN,TRIETHANOLAMINE,SODIUM HYALURONATE,DISODIUM EDTA

stop use

on broken or irritated scalp

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WHITENING AND ANTI-FRECKLE ESSENCE 
whitening and anti-freckle essence liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84372-056
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84372-056-01	30 g in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	09/11/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/11/2024

Labeler - Shenzhen Zhumeng Times Technology Co., Ltd. (631852731)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Zhumeng Times Technology Co., Ltd.		631852731	manufacture(84372-056)