AQUAX WHITENING- oligopeptide-68 cream

Aquax Whitening by

Drug Labeling and Warnings

Aquax Whitening by is a Otc medication manufactured, distributed, or labeled by Pella Pharmaceuticals Co. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• Whitening of skin.
• Reduction of spots due to sunlight exposure.
• Pregnancy Mask (Melasma).
• Reduction of secular pigmentations of acne.
• Can be used on sensitive areas (armpits, genital region, knees, elbows .. etc.)
• The Product is Safe and Effective.

Precautions

Keep out of reach of children

Warnings

• For external use only
• Avoid contact with the eyes
• If you are allergic to any of the ingredients listed, you should check with your doctor or pharmacist before you use the product.

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

Secondary Package

INGREDIENTS AND APPEARANCE

AQUAX WHITENING 
oligopeptide-68 cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82160-245
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AMINO ACIDS (UNII: 0O72R8RF8A) (AMINO ACIDS - UNII:0O72R8RF8A)	AMINO ACIDS	0.2 mg  in 50 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82160-245-01	1 in 1 CARTON	09/13/2010
1		50 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/13/2010

Labeler - Pella Pharmaceuticals Co. Ltd (562370925)