CORRECTOR LIGHT- hydroquinone lotion

Country: Bandaríkin

Tungumál: enska

Heimild: NLM (National Library of Medicine)

Kauptu það núna

Vara einkenni Vara einkenni (SPC)
06-11-2013

Virkt innihaldsefni:

HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)

Fáanlegur frá:

Vivier Pharma, Inc.

Stjórnsýsluleið:

TOPICAL

Gerð lyfseðils:

OTC DRUG

Leyfisstaða:

OTC monograph not final

Vara einkenni

                                CORRECTOR LIGHT- HYDROQUINONE LOTION
VIVIER PHARMA, INC.
_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._
----------
CORRECTOR LIGHT
ACTIVE INGREDIENT
Hydroquinone USP (2%)
INDICATION
Skin Bleaching and Correcting
INDICATION
To gradually lighten hyperpigmentation of the skin such as age spots,
liver spots, freckles or
hyperpigmentation that can occur as a result of pregnancy or the use
of oral contraceptives.
PRECAUTIONS
For external use only. Avoid contact with eyes. If contact occurs,
rinse thoroughly with water. Keep out
of reach of children. Use only on the advice of a physician. Contains
Sodium Metabisulfite. See
package insert for complete details.
PRECAUTIONS
Keep out of reach of children.
DIRECTIONS
Use fingertips to apply a thin layer to affected areas. Use both
morning and night or as directed by a
physician. Gradual lightening of the discolored area can be expected
in most cases. Close cap securely
after each use. Store at room temperature (15-30°C / 59-86°F).
NON-MEDICINAL INGREDIENTS
Cetearyl Alcohol, Cetyl Alcohol, Disodium EDTA, Ethoxydiglycol,
Fragrance/Parfum, Glycerin,
Lactic Acid, L-Ascorbic Acid USP, Methylparaben, Phenyl Trimethicone,
PPG-2 Myristyl Ether
Propionate, Propylparaben, Sodium Cetearyl Sulfate, Sodium Lauryl
Sulfate, Sodium Metabisulfite,
Tocopheryl Acetate, Water/Eau.
PRINCIPAL DISPLAY PANEL
Corrector Light_PackageLabel_PrincipalDisplayPanel
CORRECTOR LIGHT
hydroquinone lotion
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 7226 -28 20
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
HYDRO Q UINO NE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)
HYDROQUINONE
2 g in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
CETO STEARYL ALCO HO L (UNII: 2DMT128 M1S)
CETYL ALCO HO L (UNII: 9 36 JST6 JCN)
EDETATE DISO DIUM (UNII: 7FLD9 
                                
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