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Blemish

Kamins Dermatologics Inc.
Kamins Dermatologics Inc.

BLEMISH GEL 5% CONSUMER LABELING




FULL PRESCRIBING INFORMATION

Active ingredient



Purpose



Uses

A unique oil-free, color-free benzoyl peroxide gel that helps to gently clear blemishes, blackheads and spots.  Also contains our moisturizing Bio-Maple compound, which helps prevent skin from becoming excessively dry.

Uses

■ Helps treat acne.

■ Dries up acne pimples.

■ Helps prevent new acne pimples.

Warnings

For external use only.

Do not use on

  • broken skin.
  • large areas of the body.

When using this product,

  • Apply to affected areas only
  • avoid unnecessary sun exposure and use a sunscreen
  • avoid contact with eyes/eye area, lips, mouth and nostrils.  If contact occurs, rinse thoroughly with water.
  • This product may bleach hair or dyed fabrics.
  • Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin.  Only one drug should be used unless directed by a doctor.

Stop use and ask a doctor if too much skin irritation or sensitivity develops or increases.

If swallowed, seek medical assistance or contact a Poison Control Center immediately.

Directions

  • Clean the skin thoroughly befor applying.
  • Cover the entire affected area with a thin layer 1 to 3 times daily.
  • because too much drying of the skin may occur, start with 1 application daily, then gradually increase to 2-3 times daily if needed or as directed by a doctor.
  • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • If going outside, use a sunscreen.  Allow medicated acne gel to dry, then follow directions on the sunscreen labeling.

INACTIVE INGREDIENTS: water, alcohol denat., acer saccharum (maple isolate), disodium PEG-12 dimethicone sulfosuccinate, carbomer, sodium hydroxide, phenoxyethanol, caprylyl glycol, sorbic acid

B. KAMINS

BLEMISH GEL 5%

30mL / 1.7 fl.oz

DIN 02248217Blemish

Blemish

Benzoyl peroxide GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63550-193
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZOYL PEROXIDE BENZOYL PEROXIDE 50 mg

Inactive Ingredients

Ingredient Name Strength
water
ACER SACCHARUM SAP
DIMETHICONE
SODIUM HYDROXIDE
PHENOXYETHANOL
CAPRYLYL GLYCOL
sorbic acid

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63550-193-23 30 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partD part333D 2010-10-19


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Be sure to consult your doctor before taking any medication!
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