PORCELANA DAY SKIN LIGHTENING- hydroquinone and octinoxate cream 
Ultimark Products LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Porcelana Day Skin Lightening Cream

Active Ingredient

Hydroquinone U.S.P. 2%

Purpose

Skin Lightener

Active Ingredient

Octinoxate 2.5%

Purpose

Sunscreen

Uses:

Warnings

For External use only. Avoid contact with eyes. Some users of this product may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a doctor.

Do Not use on

children under 12 years of age unless directed by a doctor.

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a doctor before use.

Questions or Comments?

Call 1-800-820-8717

Monday - Friday 9:00 - 6:00 EST or visit us at: www.nicenebrands.com

¿Las Preguntas o Comentarios? Llame al 1-800-820-8717

Lunes - Viernes 9:00 - 6:00 EST, o visítenos en:

www.nicenebrands.com

Directions

Inactive Ingredients

Water, Mineral Oil, Glyceryl Stearate, Cetyl Alcohol, Isopropyl Palmitate, PEG-100 Stearate, Propylene Glycol, Emulsifying Wax NF, Stearic Acid, Hydroxyethylcellulose, Tocopheryl Acetate, Magnesium Ascorbyl Phosphate, Beta-Carotene, Disodium EDTA, C13-14 Isoparaffin, Sodium Meta-Bisulfite, Citric Acid, BHT, Methylparaben, Propylparaben, Diazolidinyl Urea, Fragrance.  

PRINCIPAL DISPLAY PANEL

PORCELANA®
FOR BALANCED SKIN TONE

DAY

SKIN LIGHTENING CREAM

FADES DARK SPOTS
      EVENS SKIN TONE
Protects With
Anti-Oxidants & Sunscreen
      Net Wt 3 oz/85 g

PRINCIPAL DISPLAY PANEL
PORCELANA®
FOR BALANCED SKIN TONE
DAY
SKIN LIGHTENING CREAM
FADES DARK SPOTS	EVENS SKIN TONE
Protects With
Anti-Oxidants & Sunscreen	Net Wt 3 oz/85 g

PORCELANA DAY SKIN LIGHTENING 
hydroquinone and octinoxate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51545-110
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE0.02 g  in 1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.025 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MINERAL OIL (UNII: T5L8T28FGP)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
.BETA.-CAROTENE (UNII: 01YAE03M7J)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51545-110-031 in 1 BOX12/14/2017
185 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A04/01/2011
Labeler - Ultimark Products LLC (964734078)
Registrant - Humco Holding Group, Inc. (825672884)

Revised: 12/2017
Document Id: 604e5e57-3b7f-3da0-e053-2991aa0a55f8
Set id: 73f8a8a2-7cec-454a-91d1-3c25d525de9a
Version: 3
Effective Time: 20171214
 
Ultimark Products LLC