SNOW WHITE SPOT- niacinamide gel

SNOW WHITE SPOT by

Drug Labeling and Warnings

SNOW WHITE SPOT by is a Otc medication manufactured, distributed, or labeled by Zenpia, EZEKIELCOSMETIC CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

niacinamide

INACTIVE INGREDIENT

Water, Butylene Glycol, Aloe Barbadensis Leaf Juice, Sodium Hyaluronate, Caprylyl Glycol, 1,2-Hexandiol, Hydrolyzed Collagen, Carbomer, Trehalose, PEG-60 Hydrogenated Castor Oil, Potassium Hydroxide, Portulaca Oleracea Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Malpighia Emarginata (Acerola) Fruit Extract, Houttuynia Cordata Extract, Morus Alba Bark Extract, Chamomilla Recutita (Matricaria) Flower Extract, Allantoin, Dipotassium Glycyrrhizate, Magnesium Ascorbyl Phosphate, Fragrance, Disodium EDTA, Tocopheryl Acetate, Retinyl Palmitate

PURPOSE

skin whitening

KEEP OUT OF REACH OF CHILDREN

keep out or reach of the children

INDICATIONS & USAGE

Take an appropriate amount and spread on to your skin and tap it.

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SNOW WHITE SPOT 
niacinamide gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70825-0009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70825-0009-1	65 g in 1 TUBE; Type 0: Not a Combination Product	07/11/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/05/2015

Labeler - Zenpia (557799448)

Registrant - Zenpia (557799448)

Establishment
Name	Address	ID/FEI	Business Operations
Zenpia		557799448	label(70825-0009)

Establishment
Name	Address	ID/FEI	Business Operations
EZEKIELCOSMETIC CO.,LTD		689851966	manufacture(70825-0009)