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Name:Sunvanish
Manufacturer:Glytone
Category:Prescription Marketed Drugs


Glytone skin Bleaching sunvanish

SUNVANISH  - hydroquinone cream 
Glytone

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.

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Glytone skin Bleaching sunvanish



Dosage Apply SunVanish in the morning to the affected area or as directed by your physician.



Warnings Contains sodium Metabisulfite, a sulfite that may cause serious allergic type reactions (eg hives, itching, wheezing, anaphylaxis, severe asthma attack) in certain susceptible persons.

For external use only



Distributed by

Genesis Pharmaceuticals Inc

Parsippany, NJ  07054

Made in USA

18004598663

www.glytone.com



Keep out of reach of children



Contains Each gram of SunVanish contains 40 mg of hydroquinone USP, 75 mg of octinoxate and 50 mg of oxybenzone in a cream base of purified water, proplyene glycol, cetostearyl alcohol, glycerin, isopropyl palmitate, sodium metabisulfite, sodium lauryl sulfate, and sorbic acid

sunvanish label


Glytone skin bleaching sunvanish with sunscreen

hydroquinone USP, 4%

RX only

Net wt 2 oz (56 g)


SUNVANISH 
hydroquinone cream
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:64760-201
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Hydroquinone (Hydroquinone) Hydroquinone 40 mg  in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER  
PROPYLENE GLYCOL  
CETOSTEARYL ALCOHOL  
GLYCERIN  
ISOPROPYL PALMITATE  
SODIUM METABISULFITE  
SODIUM LAURYL SULFATE  
SORBIC ACID  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:64760-201-01 1 TUBE ( TUBE) in 1 BOX contains a TUBE
1 56 g in 1 TUBE This package is contained within the BOX (64760-201-01)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part358A 10/01/2009

Labeler - Glytone (117196928)

Revised: 01/2011 Glytone



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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