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Neutrogena

Neutrogena Corporation

Clear Pore Oil-Eliminating Astringent


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne medication

Use

For the treatment of acne.

Warnings

For external use only

Flammable – Keep away from open fire or flame.

Ask a doctor or pharmacist before use if you are using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water.

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

Directions

  • Cleanse the skin thoroughly before applying medication.
  • Moisten a cotton ball and cover the entire affected area with a thin layer one to three times daily.
  • Do not rinse.
  • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three 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.

Inactive ingredients

Alcohol Denat. (45%)
Water
Witch Hazel (Hamamelis Virginiana) Extract
Butylene Glycol
Glycereth-7
Aloe Barbadensis Leaf Extract
Matricaria (Chamomilla Recutita) Flower Extract
Methyl Gluceth-20
Benzophenone-4
Blue 1
Propylene Glycol
Fragrance

Questions?

1-800-582-4048 (USA) or www.neutrogena.com

© Dist. by
Neutrogena Corp.
Los Angeles CA 90045

PRINCIPAL DISPLAY PANEL - 236mL Bottle Label

Clear
Pore

Oil-Eliminating
Astringent

effectively treats
and helps prevent
breakouts without
overdrying

salicylic acid
acne medication

Neutrogena®

DERMATOLOGIST RECOMMENDED

8 FL OZ (236mL)

Neutrogena

Neutrogena

Salicylic Acid LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10812-973
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Salicylic Acid SALICYLIC ACID 20 mg

Inactive Ingredients

Ingredient Name Strength
water
BUTYLENE GLYCOL
Aloe Vera Leaf
CHAMOMILE
methyl gluceth-20
SULISOBENZONE
FD&C BLUE NO. 1
propylene glycol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10812-973-01 236 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partD part333D 2011-09-15


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Be sure to consult your doctor before taking any medication!
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