Friday 25 February 2011

Sulfa Quin




Sulfa Quin may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Sulfa Quin



Sulfaquinoxaline

Sulfaquinoxaline is reported as an ingredient of Sulfa Quin in the following countries:


  • Australia

International Drug Name Search

Wednesday 23 February 2011

Dilopin




Dilopin may be available in the countries listed below.


Ingredient matches for Dilopin



Amlodipine

Amlodipine is reported as an ingredient of Dilopin in the following countries:


  • Turkey

International Drug Name Search

Saturday 12 February 2011

Obagi C Rx System C Clarifying Serum



hydroquinone

Dosage Form: cream
Obagi-C Rx

OBAGI-C® RX SYSTEM


WELCOME TO THE OBAGI-C® RX SYSTEM OF SKIN CARE PRODUCTS!



PATIENT INFORMATION


FOR TOPICAL USE ONLY


With Obagi-C Rx, you’re on your way to healthier, refreshed, revitalized skin from cell to surface. Obagi-C Rx Systems promote skin rejuvenation from the inside out using a formulation of prescription-strength hydroquinone USP, 4%, which reduces the appearance of hyperpigmentation and age spots, combined with 10% L-ascorbic acid (Vitamin C)—the only topical antioxidant proven to stimulate collagen synthesis and protect your skin by minimizing future skin cell damage.


Please read this product information prior to use of the Obagi-C Rx System. Any questions regarding your particular skin care regimen should be directed toward your physician or skin care specialist. You can also obtain more information about the Obagi-C Rx System or other Obagi systems by visiting our Web site at www.obagi.com.



PHYSICIAN PRESCRIBING INFORMATION


FOR EXTERNAL USE ONLY Rx Only


62032-106-10 OBAGI-C RX SYSTEM C-CLARIFYING SERUM FOR NORMAL TO DRY SKIN



ACTIVE INGREDIENT:


Hydroquinone USP, 4%



INACTIVE INGREDIENTS:


Ascorbic Acid, Propylene Carbonate, Propylene Glycol, Sodium Lauryl Sulfate, Water


62032-122-10 OBAGI-C RX SYSTEM C-CLARIFYING SERUM FOR NORMAL TO OILY SKIN



ACTIVE INGREDIENT:


Hydroquinone USP, 4%



INACTIVE INGREDIENTS:


Ascorbic Acid, Dipropylene Glycol, Ethyl Alcohol, Fragrance, Propylene Carbonate, Propylene Glycol, Sodium Lauryl Sulfate, Water


62032-105-36 OBAGI-C RX SYSTEM C-THERAPY NIGHT CREAM



ACTIVE INGREDIENT:


Hydroquinone USP, 4%



INACTIVE INGREDIENTS:


Ascorbic Acid, BHT, Cetyl Alcohol, Disodium EDTA, Glycerin, Lactic Acid, Methylparaben, Phenyl Trimethicone, PPG-2 Myristyl Ether Propionate, Propylparaben, Saponins, Sodium Lauryl Sulfate, Sodium Metabisulfite, TEA-Salicylate, Tocopheryl Acetate, Water



DESCRIPTION


Hydroquinone is 1,4-benzenediol. Hydroquinone occurs as fine, white needles. The drug is freely soluble in water and in alcohol. Chemically, hydroquinone is designated as p-dihydroxybenzene; the empirical formula is C6H6O2; molecular weight is 110.11 g/mol. The chemical structure is in diagram to right. 


 



CLINICAL PHARMACOLOGY


Topical application of hydroquinone produces a reversible depigmentation of the skin by inhibition of the enzymatic oxidation of tyrosine to 3, 4-dihydroxyphenylalanine (dopa) and suppression of other melanocyte metabolic processes. Exposure to sunlight or ultraviolet light will cause repigmentation of the bleached areas, which may be prevented by the use of sunblocking agents or sunscreen agents contained in the Obagi-C Rx System C-SunGuard SPF 30.



INDICATIONS AND USAGE


The gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation.



DOSAGE AND ADMINISTRATION


A thin application should be applied to the affected area twice daily or as directed by a physician. If no improvement is seen after 8‑12 weeks of treatment, use of this product should be discontinued. Sun exposure should be limited by using a sunscreen agent, a sunblocking agent, or protective clothing to cover bleached skin when using and after using this product in order to prevent repigmentation.



WARNINGS


  • Hydroquinone is a skin-bleaching agent, which may produce unwanted cosmetic effects if not used as directed. The physician should be familiar with the contents of this insert before prescribing or dispensing this medication.

  • Test for skin sensitivity before using by applying a small amount to an unbroken patch of skin and check within 24 hours. Minor redness is not a contraindication, but where there is itching or vesicle formation or excessive inflammatory response, product should be discontinued and physician consulted. Close patient supervision is recommended.

  • Avoid contact with eyes, nose, mouth, or lips. In case of accidental contact, patient should rinse eyes, nose, mouth, or lips with water and contact physician.

  • Sunscreen use is an essential aspect of hydroquinone therapy because even minimal sunlight exposure sustains melanocytic activity.

  • The Obagi-C Rx System C-Therapy Night Cream contains sodium metabisulfite, a sulfite that may cause serious allergic-type reactions (e.g., hives, itching, wheezing, anaphylaxis, severe asthma attacks) in certain susceptible persons.


PRECAUTIONS


(ALSO SEE WARNINGS)


Treatment should be limited to relatively small areas of the body at one time since some patients experience a transient skin reddening and a mild burning sensation, which does not preclude treatment.



PREGNANCY CATEGORY C


Animal reproduction studies have not been conducted with topical hydroquinone. It is also not known whether hydroquinone can cause fetal harm when used topically on a pregnant woman or affect reproductive capacity. It is not known to what degree, if any, topical hydroquinone is absorbed systemically. Topical hydroquinone should be used on pregnant women only when clearly indicated.



NURSING MOTHERS


It is not known whether topical hydroquinone is absorbed or excreted in human milk. Caution is advised when topical hydroquinone is used by a nursing mother.



PEDIATRIC USAGE


Safety and effectiveness in children below the age of 12 years have not been established.



ADVERSE REACTIONS


No systemic adverse reactions have been reported. Occasional hypersensitivity (localized contact dermatitis) may occur, in which case the product should be discontinued and physician notified immediately.



CONTRAINDICATIONS


People with prior history of sensitivity or allergic reaction to this product or any of its ingredients should not use it. The safety of topical hydroquinone use during pregnancy or in children (12 years and under) has not been established.



HOW SUPPLIED


  • The Obagi-C Rx System C-Clarifying Serum (Hydroquinone USP, 4%) for Normal to Dry Skin is available as follows: 1 fl. oz. (30 mL) bottle NDC 62032-106-10

  • The Obagi-C Rx System C-Clarifying Serum (Hydroquinone USP, 4%) for Normal to Oily Skin is available as follows: 1 fl. oz. (30 mL) bottle NDC 62032-122-10

  • The Obagi-C Rx System C-Therapy Night Cream (Hydroquinone USP, 4%) is available as follows: 2 oz. (57 g) bottle NDC 62032-105-36

Store at controlled room temperature: 15°-25°C (59°-77°F), and keep out of direct sunlight.


Obagi Medical Products, Inc. Long Beach, CA 90806, U.S.A. www.obagi.com 60501510X Patent #4,983,382; 5,516,793; 5,703,122; 6,299,889 - Rev. 02/10



PRINCIPAL DISPLAY PANEL


OBAGI-C®

RX SYSTEM

NDC # 62032-122-10

NON-COMEDOGENIC

NON-ACNEGENIC

C-CLARIFYING SERUM

SKIN LIGHTENING SERUM

WITH VITAMIN C 10%

HYDROQUINONE USP, 4%

RX ONLY

FOR NORMAL TO OILY SKIN

AM

1 FL. OZ. (30 Ml)










Obagi C Rx System C Clarifying Serum 
hydroquinone  cream










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)62032-122
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE)HYDROQUINONE1.26 g  in 30 mL


















Inactive Ingredients
Ingredient NameStrength
ASCORBIC ACID 
PROPYLENE CARBONATE 
PROPYLENE GLYCOL 
SODIUM LAURYL SULFATE 
WATER 
DIPROPYLENE GLYCOL 
ALCOHOL 


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
162032-122-1030 mL In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
UNAPPROVED DRUG OTHER08/31/2010


Labeler - Obagi Medical Products, Inc. (790553353)









Establishment
NameAddressID/FEIOperations
PureTek Corporation785961046LABEL, MANUFACTURE, PACK
Revised: 01/2011Obagi Medical Products, Inc.

More Obagi C Rx System C Clarifying Serum resources


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Tuesday 8 February 2011

Eritromicina Etilsuccinato Induquimica




Eritromicina Etilsuccinato Induquimica may be available in the countries listed below.


Ingredient matches for Eritromicina Etilsuccinato Induquimica



Erythromycin

Erythromycin ethylsuccinate (a derivative of Erythromycin) is reported as an ingredient of Eritromicina Etilsuccinato Induquimica in the following countries:


  • Peru

International Drug Name Search