Nizoral description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Nizoral

McNeil Consumer Healthcare Div. McNeil-PPC, Inc

Nizoral A-D KETOCONAZOLE SHAMPOO 1%


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Ketoconazole 1%

Purpose

Anti-dandruff shampoo

Nizoral Uses

controls flaking, scaling and itching associated with dandruff

Warnings

For external use only

Do not use

  • on scalp that is broken or inflamed
  • if you are allergic to ingredients in this product

When using this product

  • avoid contact with eyes
  • if product gets into eyes, rinse thoroughly with water

Stop use and ask a doctor if

  • rash appears
  • condition worsens or does not improve in 2-4 weeks

If pregnant or breast-feeding, ask a doctor before use

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

Directions

adults and children 12 years and over
  • wet hair thoroughly
  • apply shampoo, generously lather, rinse thoroughly. Repeat
  • use every 3-4 days for up to 8 weeks or as directed by a doctor. Then use only as needed to control dandruff.
children under 12 years
  • ask a doctor

Nizoral Other information

  • store between 35° and 86°F (2° and 30°C)
  • protect from light
  • protect from freezing
  • see top panel for lot number and expiration date

Inactive ingredients

acrylic acid polymer (carbomer 1342), butylated hydroxytoluene, cocamide MEA, FD&C Blue #1, fragrance, glycol distearate, polyquaternium-7, quaternium-15, sodium chloride, sodium cocoyl sarcosinate, sodium hydroxide and/or hydrochloric acid, sodium laureth sulfate, tetrasodium EDTA, water-

Questions or comments?

call 1-800-962-5357

PRINCIPAL DISPLAY PANEL

NON-PRESCRIPTION STRENGTH

NDC 50580-895-04

Nizoral®
A-D KETOCONAZOLE SHAMPOO 1%

Anti-Dandruff
Shampoo

CONTROLS FLAKING,
SCALING AND ITCHING

The Freedom Will Go To Your Head

4 FL OZ (125 mL)

Nizoral

Nizoral

Ketoconazole SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50580-895
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
KETOCONAZOLE KETOCONAZOLE 10 mg

Inactive Ingredients

Ingredient Name Strength
CARBOMER 1342
BUTYLATED HYDROXYTOLUENE
COCO MONOETHANOLAMIDE
FD&C BLUE NO. 1
GLYCOL DISTEARATE
HYDROCHLORIC ACID
quaternium-15
SODIUM CHLORIDE
SODIUM HYDROXIDE
SODIUM LAURETH SULFATE
EDETATE SODIUM
water

Product Characteristics

Color
BLUE (opaque, pearlescent blue to blue green)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 125 in 1 BOTTLE
2 200 in 1 BOTTLE
3 125 in 1 BOTTLE
4 6 in 1 PACKET
5 NDC:50580-895-15 10 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020310 1999-04-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.