SNOW WHITE MILKY PACK- niacinamide cream 
Zenpia

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

niacinamide

Water,Cyclopentasiloxan,Cyclohexasiloxan,Dimethicon,Cyclomethicon,Butylene Glycol,Cetyl PEG/PPG-10/1 Dimethicone,Dimethicone/Vinyl Dimethicone Crosspolymer,IsoDodecan,Disteardimonium Hectorite,Propylene Carbonate,Titanium Dioxide,Mica,Polymethyl Methacrylate,CI 77492,CI 77499,Triethoxycaprylylsilane,Sodium Hyaluronate,Sorbitan Sesquioleate,Ceresin,Magnesium Sulfate,Phenoxyethanol,Disodium EDTA,Fragrance

skin whitening

keep out or reach of the children

Apply onto cleaned face or body and gently massage it.

Wash off it with warm water after 2-3 minutes.

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

for external use only


label

SNOW WHITE MILKY PACK 
niacinamide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70825-0008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70825-0008-1200 g in 1 TUBE; Type 0: Not a Combination Product07/11/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/05/2015
Labeler - Zenpia (557799448)
Registrant - Zenpia (557799448)
Establishment
NameAddressID/FEIBusiness Operations
Zenpia557799448label(70825-0008)
Establishment
NameAddressID/FEIBusiness Operations
EZEKIELCOSMETIC CO.,LTD689851966manufacture(70825-0008)

Revised: 12/2018
Document Id: 7d5da4fc-c001-3aba-e053-2a91aa0a46cb
Set id: 383ce892-de5c-62e8-e054-00144ff88e88
Version: 2
Effective Time: 20181219
 
Zenpia