SUPERLIGHTENER hydroquinone gel

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

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

Available from:

CoValence Inc

INN (International Name):

HYDROQUINONE

Composition:

HYDROQUINONE 20 mg in 1 g

Prescription type:

OTC DRUG

Authorization status:

OTC monograph not final

Summary of Product characteristics

                                SUPERLIGHTENER - HYDROQUINONE GEL
COVALENCE 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._
----------
SKINTINU Bright White Serum/2% HQ
ACTIVE INGREDIENTS: Hydroquinone (2%)
PURPOSE: Skin Lightener
Keep out of reach of children. If swallowed, immediately get medical
help or contact Poison Control
Center.
Use of this product should be discontinued if no improvement is seen
after 3 months. Lightening effect
of this product may not be noticeable when used on dark skin.
WARNINGS: For external use only. Do not use in or near eyes. If
contact occurs, rinse thoroughly with
water. Mild skin irritation may occur. Stop use if irritation is
severe.
SUN WARNING: This product contains an alpha and/or beta hydroxy acid
(AHA/BHA) that may increase
your skin sensitivity to sunlight and the risk of sunburn. Wear
sunscreen and reduce sun exposure while
using this product and a week afterwards.
INSTRUCTIONS: Apply a small amount as a thin layer on the affected
areas twice daily or use as directed
by doctor.
INACTIVE INGREDIENTS: Glycerin, Alcohol Denat., Azelaic Acid,
Hamamelis Virginiana (Wtich Hazel)
Water, Aqua (Water), Lactic Acid, Kojic Acid, Ascorbic Acid, Salicylic
Acid, Hydroxypropyl
Methylcellulose, Sodium Chloride, Sodium Hydroxide
SKINTINU Bright White Serum/2% HQ
SUPERLIGHTENER
hydroquinone gel
PRODUCT INFORMATION
CoValence Inc
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 6 9 15-413
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
20 mg in 1 g
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:6 6 9 15-413-0 4
1 in 1 CARTON
1
NDC:6 6 9 15-413-0 3
30 g in 1 BOTTLE, GLASS
2
NDC:6 6 9 15-413-10
378 5 g in 1 BOTTLE, PLASTIC
3
NDC:6 6 9 15-413-0 5
1 in 1 CA
                                
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