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Neutrogena

Neutrogena Corporation

Neutrogena Clear Pore Daily Scrub


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Benzoyl Peroxide 3.7%

Purpose

Acne medication

Use

For the treatment of acne

Warnings

For external use only

When using this product

  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Do not use if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

When using this product

  • avoid unnecessary sun exposure and use sunscreen
  • avoid contact with the eyes, lips, and mouth
  • avoid contact with hair and dyed products, which may be bleached by this product
  • skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration

Stop use and ask a doctor if

  • irritation becomes severe

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Products, such as soaps and masks, may be applied removed and should include appropriate directions

  • If going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor

Inactive ingredients

Water, Glycerin, Kaolin, Bentonite, Sodium Methyl Cocoyl Taurate, Titanium Dioxide, Polyethylene, Sodium Chloride, Xanthan Gum, Citric Acid, Sodium Citrate, Trideceth-9, Disodium EDTA, Fragrance, PEG-5 Ethylhexanoate, and Menthol

Questions or comments?

1-800-582-4048 (USA only)

  • Avoid storage at extreme temperatures (below 40°F and above 100°F).

PRINCIPAL DISPLAY PANEL - 125 Bottle Label

NEW

Clear
Pore

Daily Scrub

Benzoyl peroxide formula
penetrates pores to kill
breakout-causing bacteria

Neutrogena®

benzoyl peroxide acne medication

4.2 FL OZ (125 mL)

Neutrogena

Neutrogena

Benzoyl Peroxide CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10812-404
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BENZOYL PEROXIDE BENZOYL PEROXIDE 37 mg

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
KAOLIN
BENTONITE
titanium dioxide
SODIUM CHLORIDE
XANTHAN GUM
CITRIC ACID MONOHYDRATE
SODIUM CITRATE
EDETATE DISODIUM
MENTHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10812-404-01 125 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partD part333D 2010-12-01


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Be sure to consult your doctor before taking any medication!
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