Rite Aid Dandruff description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Rite Aid Dandruff

Rite Aid Corporation
APOLLO HEALTH AND BEAUTY CARE

Drug Facts - Back Label


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Pyrithione Zinc 1%

Purpose

Anti-dandruff

Rite Aid Dandruff Uses

Helps prevent recurrence of flaking and itching associated with dandruff

Warnings

For external use only

When using this product

Avoid contact with eyes. If contact occurs, rinse eyes with water thoroughly

Stop use and ask doctor if

Conditions worsens or does not improve after regular use of this product as directed

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • Shake well, wet hair, massage onto scalp, rinse. Repeat if desired.
  • For best results use at least twice a week or as directed by a doctor.
  • For maximum dandruff control, use every time you shampoo

Inactive Ingredients

Water, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Glycol Distearate, Dimethicone, Zinc Carbonate, Fragrance, Cetyl Alcohol, Polyquaternium-10, Magnesium Sulfate, Sodium Benzoate, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Benzyl Alcohol, Sodium Chloride, Elaeis Guineensis (Palm) Oil, Sodium Xylenesulfonate, Aloe Barbadensis Leaf, Anthemis Nobilis Flower Oil, Tocopheryl Acetate, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 10

Principle Display Panel

Rite Aid Dandruff dry scalp care

Large Size

Compare to Head and Shoulder®

2 in 1 Dry Scalp Care

Dandruff Shampoo plus Conditioner

For normal or dry hair

15.2 FL OZ (449 mL)

ra.jpg Rite Aid Dandruff

Rite Aid Dandruff

Pyrithione Zinc SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11822-4111
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC 1 mL

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURETH SULFATE
SODIUM LAURYL SULFATE
COCO MONOETHANOLAMIDE
GLYCOL DISTEARATE
DIMETHICONE
ZINC CARBONATE
CETYL ALCOHOL
MAGNESIUM SULFATE ANHYDROUS
SODIUM BENZOATE
ALMAGATE
AMMONIUM LAURETH-2 SULFATE
BENZYL ALCOHOL
SODIUM CHLORIDE
palm oil
Aloe Vera Leaf
CHAMAEMELUM NOBILE FLOWER OIL
ALPHA-TOCOPHEROL ACETATE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
D&C YELLOW NO. 10

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11822-4111-5 449 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2010-10-20


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.