AQUAX WHITENING- oligopeptide-68 cream 
Pella Pharmaceuticals Co. Ltd

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.

----------

Whitening

Forms and presentation

Cream: Tube of 50 g.

Active Ingredient

Oligopeptide-68

Inactive Ingredients

Aqua, Glycerin, Celyl Alcohol, Polysorbate 80, Cera Alba, Butylene Glycol, Xanthan Gum, Carbomer, Methylparaben, Triethanolamine, Propylparaben, Parfum, Hydrogenated Lecithin, Glycine Soja, Sodium Oleat, Disodium EDTA and BHA.

Purpose

Whitening

Properties

Aquax ® Whitening is a cream that moisturizes, nourishes and lightens skin.

Indications

Precautions

Keep out of reach of children

Warnings

Contraindications

Hypersensitivity to any of the components.

Side effects

Aquax ® Whitening Cream has no known side effect, because using it is safe.

Dosage and administration

Apply Aquax ® Whitening Cream twice daily (morning and evening) on a cleaned skin.

Storage conditions

Store at a temperature below 30 ° C.

Primary Package

Primary Package

Secondary Package

Secondary Package

AQUAX WHITENING 
oligopeptide-68 cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82160-245
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMINO ACIDS (UNII: 0O72R8RF8A) (AMINO ACIDS - UNII:0O72R8RF8A) AMINO ACIDS0.2 mg  in 50 g
Inactive Ingredients
Ingredient NameStrength
SOYBEAN OIL (UNII: 241ATL177A)  
WHITE WAX (UNII: 7G1J5DA97F)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
TROLAMINE (UNII: 9O3K93S3TK)  
SODIUM OLEATE (UNII: 399SL044HN)  
GLYCERIN (UNII: PDC6A3C0OX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
XANTHAN GUM (UNII: TTV12P4NEE)  
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82160-245-011 in 1 CARTON09/13/2010
150 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/13/2010
Labeler - Pella Pharmaceuticals Co. Ltd (562370925)

Revised: 12/2021
Document Id: d227b8f3-fc50-06b8-e053-2a95a90a5a1d
Set id: d227b8f3-fc4f-06b8-e053-2a95a90a5a1d
Version: 245
Effective Time: 20211202
 
Pella Pharmaceuticals Co. Ltd