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 Volume


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Pyrithione zinc 1%

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.
  • shake before use.
  • wet hair, massage onto scalp, rinse, repeat if desired.

Inactive ingredients

Water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, zinc carbonate, sodium chloride, sodium xylenesulfonate, cocamidopropyl betaine, fragrance, dimethicone, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, methylchloroisothiazolinone, methylisothiazolinone.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 700 mL Bottle Label

NEW
fresh scent
technology

head &
shoulders®

pyrithione zinc dandruff shampoo

extra volume

24 hour volume boost

FLAKE FREE.*
100%
GUARANTEED^

23.7 FL OZ
(700 mL)

96305397

Head and Shoulders

Head and Shoulders

Pyrithione Zinc LOTION/SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37000-082
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC 10 mg

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURYL SULFATE
SODIUM LAURETH-3 SULFATE
GLYCOL DISTEARATE
ZINC CARBONATE
SODIUM CHLORIDE
SODIUM XYLENESULFONATE
COCAMIDOPROPYL BETAINE
DIMETHICONE
SODIUM BENZOATE
MAGNESIUM CARBONATE HYDROXIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37000-082-42 420 in 1 BOTTLE, PLASTIC
2 NDC:37000-082-70 700 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2013-09-01


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Be sure to consult your doctor before taking any medication!
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