Thursday 8 September 2016

Bencort Lotion



benzoyl peroxide and hydrocortisone

Dosage Form: lotion, kit
Bencort Lotion Kit

INDICATIONS AND USAGE:


For the treatment of acne vulgaris.

Bencort Lotion Dosage and Administration


Shake well before use. Apply a thin film, 1 to

3 times daily, gently massaging into skin or as directed by a physician.



TO THE PHARMACIST


At the time of dispensing, add the contents of the

Bencort Benzoyl Peroxide Powder vial to the Bencort Lotion in the bottle.

Shake well to ensure uniform dispersion. Place expiration date of three (3) months on

the label. Bencort Lotion is 25 grams net weight.



Contraindications


Bencort Lotion is contraindicated in patients

hypersensitive to benzoyl peroxide, hydrocortisone, other corticosteroids or to any

ingredient contained in this product. Topical steroids are contraindicated in viral

diseases of the skin, such as varicella or vaccinia. Topical corticosteroids should not

be used in patients with markedly impaired circulation since skin ulceration has

occurred in these patients following use of the drugs.



Warnings and Precautions


Irritation including peeling, itching and/or redness

may occur, especially at the start of treatment. If any of these effects persist or worsen,

stop using and contact your doctor immediately. Smaller amounts of the drug may need to

be applied less often. Consult your doctor for instructions. For external use only. Keep away

from the eyes and mucous membranes. If severe irritation or swelling develops, discontinue

use and seek appropriate therapy.



Adverse Reactions


The most frequent adverse reactions to benzoyl peroxide

are irritation and contact dermatitis. Although 0.5% hydrocortisone is considered

safe, the following adverse reactions have been reported with topical corticosteroids,

especially under occlusive dressings: burning, itching, irritation, dryness, folliculitis,

hypertrichosis, acneform eruptions, hypopigmentation, perioral dermatitis, allergic

contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae,

miliaria.


This is not a complete list of possible adverse effects. If you notice other effects not

listed above, contact your doctor or pharmacist.


Call your doctor for medical advice about side effects. You may

report side effects to the FDA at 1-800-FDA-1088.



Drug Interactions


Before using this medication, tell your doctor or

pharmacist of all prescription and nonprescription products you currently use.



USE IN SPECIFIC POPULATIONS


Pregnancy, Category C: Animal reproduction studies have not been conducted

with Bencort Lotion. It is also not known whether Bencort Lotion can cause

fetal harm when administered to pregnant women or affect reproduction capacity.

Bencort Lotion should be given to pregnant women only if clearly needed.


Nursing Mothers: It is not known whether this drug is excreted in human milk.

Because many drugs are excreted in human milk, caution should be exercised when

Bencort Lotion is administered to nursing women.


Pediatric Use: Safety and effectiveness in pediatric patients below the age of 12

have not been established.



Overdosage


This medication may be harmful if swallowed. If swallowing or

overdose is suspected, contact your local poison control center or emergency room

immediately or the National Poison Hotline at 1-800-222-1222.



Bencort Lotion Description


Bencort Lotion (benzoyl peroxide 5% and hydrocortisone 0.5%)

TOPICAL LOTION. Each gram contains, as dispensed, 50 mg benzoyl peroxide and 5 mg

hydrocortisone.Inactive Ingredients: acetylated lanolin alcohol, BHA, C12-15 alkyl

benzoate, cetyl acetate, cetyl alcohol, citric acid, decyl oleate, dioctyl sodium

sulfosuccinate, EDTA, elaeis guineensis (palm) fruit extract, glycine soja (soybean) seed

extract, hydroxyethylcellulose, lanolin oil, methylparaben, mineral oil, oleyl acetate,

oryzanol, pentasodium pentetate, polysorbate 20, PPG-5-ceteth-20, propyl gallate,

propylene glycol, propylene glycol stearate, propylparaben, purified water (aqua), silica,

simethicone, sodium phosphate, stearyl acetate, stearyl heptanoate, tetrasodium EDTA,

tricalcium phosphate, trisodium phosphate.


The structural formula for benzoyl peroxide (Mol. Formula: C14H10O4; Mol. Weight

242.23):



The structural formula for hydrocortisone, pregn-4-ene-3,20-dione, 11,17,21-

trihydroxy-,(11b)- (Mol. Formula: C21H30O5; Mol. Weight 362.47 ):





Bencort Lotion - Clinical Pharmacology


Benzoyl peroxide is an antibacterial agent shown

to be effective against P. acnes. The antibacterial action of benzoyl peroxide is believed

to be due to the release of reactive oxygen species. Benzoyl peroxide has a keratolytic

effect which may contribute to its efficacy. Benzoyl peroxide has been shown to be

absorbed by the skin where it is converted into benzoic acid.


Hydrocortisone shares the actions of other topical corticosteroids and are used for their

anti-inflammatory and vasoconstrictive actions.

NONCLINICAL TOXICOLOGY – Carcinogenesis, Mutagenesis, Impairment of Fertility:


Long-term studies in animals have not been performed to

evaluate carcinogenic potential.



How Supplied/Storage and Handling


Bencort Lotion is

supplied as bottles, 25 grams net weight as dispensed, NDC 68032-303-91. Package

contains a bottle of Bencort Lotion, net weight 21.2 grams and a vial of Bencort

Benzoyl Peroxide Powder containing a mixture of 35% benzoyl peroxide. The

inactive ingredients are tricalcium phosphate, silica and dioctyl sodium sulfosuccinate.

Net weight of vial is 3.8 grams. Keep bottle tightly closed.

Store at room temperature 20°-25°C (68°-77°F). Do not freeze.


Caution: Federal law prohibits dispensing without prescription.


KEEP THIS AND ALL MEDICATIONS OUT OF REACH OF CHILDREN


Manufactured for:

River’s Edge

Pharmaceuticals, LLC

Suwanee, GA 30024

303-11

Iss. 02/09

PACKAGING


Rx Only

NDC: 68032-419-92


Bencort Lotion Kit

(benzoyl peroxide 5% and hydrocortisone 0.5%)


Kit Contains:

•    Becort Lotion 25g (as dispensed)

•    Benzoyl Peroxide 35% Powder (to be added to the Bencort Lotion)

•    Bencort Glycerin Cleansing Lotion 60g

•    Product Information


Combined NEW WT 85g (3 oz.)


Indications: An aid in the treatment of acne.


DOSAGE AND ADMINISTRATION: Shake well before use. Apply a thin film 1 to 3 times daily, gently messaging into skin or as directed by a physician.


TO THE PHARMACIST: At the time of dispensing, add the contents of the Bencort Benzoyl Powder vial to the Bencort Hydrocortisone Lotion in the bottle. Shake well to ensure uniform dispersion. Place expiration date of three (3) months on the label. Bencort Lotion is 25g net weight, as dispensed.


Caution: Federal law prohibits dispensing without a prescription.


•    Keep away from eyes. FOR TOPICAL USE ONLY. Not for ophthalmic, oral, or intravaginal use.

•    Keep out of reach of children

•    Keep bottle tightly closed.

•    Store at room temperature 20-25C (68-77F). Do not freeze.


Consult package insert for complete prescribing information.


Apply with caution to the neck and/or other sensitive areas. There may be a slight transitory stinging or burning sensation on initial applications. Colored or dyed garments and linens may be bleached by the benzoyl peroxide.


If irritation or sensitivity occurs, discontinue use and consult your physician.


Manufactured for:

River’s Edge Pharmaceuticals, LLC

Suwanee, GA 30024

Iss. 10/09
























BENCORT 
Bencort Lotion  kit






Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68032-419










Packaging
#NDCPackage DescriptionMultilevel Packaging
168032-419-921 CARTON In 1 KITNone











QUANTITY OF PARTS
Part #Package QuantityTotal Product Quantity
Part 11 VIAL  3.8 g
Part 21 TUBE  25 g



Part 1 of 2
BENCORT 
benzoyl peroxide powder  powder










Product Information
NDC Product Code (Source)68032-303  
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE)BENZOYL PEROXIDE35   in 3.8 g





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
168032-303-213.8 g In 1 VIALNone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/01/2009




Part 2 of 2
BENCORT 
benzoyl peroxide 5% and hydrocortisone 0.5% lotion  lotion










Product Information
NDC Product Code (Source)68032-303  
Route of AdministrationTOPICALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE)BENZOYL PEROXIDE5   in 25 g
HYDROCORTISONE (HYDROCORTISONE)HYDROCORTISONE0.5   in 25 g





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
168032-303-1125 g In 1 TUBENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/01/2009











Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/01/2009


Labeler - River's Edge Pharmaceuticals, LLC (133879135)
Revised: 12/2009River's Edge Pharmaceuticals, LLC

More Bencort Lotion resources


  • Bencort Lotion Side Effects (in more detail)
  • Bencort Lotion Use in Pregnancy & Breastfeeding
  • Bencort Lotion Drug Interactions
  • Bencort Lotion Support Group
  • 0 Reviews for Bencort - Add your own review/rating


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