Hair and Scalp anti-dandruff description, usages, side effects, indications, overdosage, supplying and lots more!

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Hair and Scalp anti-dandruff

Greenbrier International
NINGBO PULISI DAILY CHEMICAL PRODUCTS CO., LTD.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient


Active Ingredient                                     Purpose

Zinc Pyrithione       1%                            Anti-dandruff


Purpose

Help prevent recurrence of flaking and itching associated with dandruff.

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

Do not get into eyes, if contact occurs, rinse eyes thoroughly with water.

Uses

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.

For external use only.

Stop use and ask a doctor if Condition worsens or does not improve after regular use as directed.

apply as needed.

water, sodium laureth sulfate, cocamidopropyl betaine, sodium lauroamphoacetate, glycol stearate, acrylates/acrylamide copolymer, ammonium chloride, methylchloroisothiazolinone, methylisothiazolinone, fragrance, citric acid, guar hydroxypropyltrimonium chloride, titanium dioxide, disodium EDTA, zinc chloride, blue 1, yellow 5

Hair and Scalp anti-dandruff

PYRITHIONE ZINC SHAMPOO

Product Information

Product Type Human otc drug label Item Code (Source) NDC:33992-1131
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC 1 g

Inactive Ingredients

Ingredient Name Strength
water
COCAMIDOPROPYL BETAINE
GLYCOL STEARATE
CARBOMER COPOLYMER TYPE A
AMMONIUM CHLORIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
CITRIC ACID MONOHYDRATE
EDETATE DISODIUM
FD&C BLUE NO. 1
FD&C YELLOW NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:33992-1131-1 400 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2013-05-08


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Be sure to consult your doctor before taking any medication!
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