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

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Head and Shoulders

Procter & Gamble Manufacturing Co.

Head and Shoulders Extra Strength


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Pyrithione zinc 2%

Purpose

Anti-dandruff

Head and Shoulders 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 thoroughly with water.

Stop use and ask a doctor if

  • condition worsens or does not improve after regular use of this product as directed.

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

Directions

  • for best results use at least twice a week or as directed by a doctor.
  • for maximum dandruff control, use every time you shampoo.
  • wet hair, massage onto scalp, rinse, repeat if desired.
  • shake before use.

Inactive ingredients

Water, sodium laureth sulfate, sodium lauryl sulfate, cocamide MEA, zinc carbonate, glycol distearate, dimethicone, sodium xylenesulfonate, fragrance, cetyl alcohol, guar hydroxypropyltrimonium chloride, magnesium sulfate, sodium chloride, sodium benzoate, magnesium carbonate hydroxide, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 420 mL Bottle Label

7
BENEFITS
no
worries from
Flakes
Itch
Breakage

head &
shoulders®

pyrithione zinc
dandruff shampoo

CLINICALLY TESTED
DANDRUFF PROTECTION

extra strength

2% pyrithione zinc

maximum strength zinc formula
without a prescription

14.2 FL OZ (420 mL)

96204110

Head and Shoulders

Head and Shoulders

Pyrithione Zinc LOTION/SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37000-059
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC 20 mg

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURETH-3 SULFATE
SODIUM LAURYL SULFATE
COCO MONOETHANOLAMIDE
ZINC CARBONATE
GLYCOL DISTEARATE
DIMETHICONE
SODIUM XYLENESULFONATE
CETYL ALCOHOL
MAGNESIUM SULFATE
SODIUM CHLORIDE
SODIUM BENZOATE
MAGNESIUM CARBONATE HYDROXIDE
BENZYL ALCOHOL
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37000-059-42 420 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2012-11-01


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Be sure to consult your doctor before taking any medication!
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