DR.ALTHEA POWER WHITENING GLUTATHIONE- niacinamide cream 
Dr. Althea

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,Butylene Glycol,Glycerin,Dimethicone,Panthenol,Titanium Dioxide (CI 77891),Niacinamide,Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Glutathione, Cyclopentasiloxane,Isohexadecane,Sodium Polyacrylate,Ethylhexyl Stearate,Polysorbate 80,Dimethiconol,Betaine,Triethoxycaprylylsilane,Trideceth-6,Pantolactone,Disodium EDTA,Phenoxyethanol,Chlorphenesin,Caprylyl Glycol,Ethylhexylglycerin,Fragrance

Helps skin whitening

keep out of reach of the children

Take appropriate amount and apply evenly to skin

1. If the following symptoms occur after product use, stop using the product immediately and consult a dermatologist (continuous use can exacerbate the symptoms).
1) Occurrence of red spots, swelling, itchiness, and other skin irritation
2) If the symptoms above occur after the application area is exposed to direct sunlight
2. Do not use on open wounds, eczema, and other skin irritations
3. Precaution for Storage and Handling
1) Close the lid after use
2) Keep out of reach of infants and children
3) Do not to store in a place with high/low temperature and exposed to direct sunlight

for external use only

label

DR.ALTHEA POWER WHITENING GLUTATHIONE 
niacinamide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70905-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70905-0002-150 mL in 1 JAR; Type 0: Not a Combination Product08/11/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/11/2016
Labeler - Dr. Althea (689694436)
Registrant - Dr. Althea (689694436)
Establishment
NameAddressID/FEIBusiness Operations
Dr. Althea689694436manufacture(70905-0002)

Revised: 8/2016
Document Id: 39d7a5d2-6797-4c08-e054-00144ff8d46c
Set id: 59fc4d3e-b555-44df-bb1a-60c7a9eac3fd
Version: 1
Effective Time: 20160812
 
Dr. Althea