Head and Shoulders 2in1 description, usages, side effects, indications, overdosage, supplying and lots more!

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Head and Shoulders 2in1

Procter & Gamble Manufacturing Co.

Head and Shoulders 2in1 Purely Gentle Scalp Care


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Pyrithione zinc 1%

Purpose

Anti-dandruff

Head and Shoulders 2in1 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 laureth sulfate, sodium lauryl sulfate, cocamide MEA, zinc carbonate, glycol distearate, dimethicone, sodium xylenesulfonate, cetyl alcohol, fragrance, guar hydroxypropyltrimonium chloride, magnesium sulfate, sodium chloride, sodium benzoate, magnesium carbonate hydroxide, aloe barbadensis leaf juice, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 700 mL Bottle Label

#1
DERM
RECOMMENDED††

head &
shoulders
®

pyrithione zinc
dandruff shampoo + conditioner

2in1
purely gentle
scalp care

clinically proven to be gentle
on scalp, and strong on dandruff

FLAKE FREE.*
100%
GUARANTEED^

aloe vera

23.7 FL OZ
(700 mL)

96260723

Head and Shoulders 2in1

Head and Shoulders 2in1

Pyrithione Zinc LOTION/SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37000-061
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 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
Aloe Vera Leaf
BENZYL ALCOHOL
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37000-061-42 420 in 1 BOTTLE, PLASTIC
2 NDC:37000-061-70 700 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2013-05-01


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