Country: United States
Language: English
Source: NLM (National Library of Medicine)
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)
CoValence Inc
HYDROQUINONE
HYDROQUINONE 20 mg in 1 g
OTC DRUG
OTC monograph not final
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 Read the complete document