VANICREAM Z-BAR- pyrithione zinc soap 
Pharmaceutical Specialties, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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VANICREAM™ Z-Bar

Drug Facts

Active Ingredient

Pyrithione zinc 2%

Purposes

Anti-dandruff,

Anti-seborrheic dermatitis

Uses

Controls and reduces the symptoms of dandruff and seborrheic dermatitis

Warnings

For external use only

Ask a doctor before use if you have a condition that covers a large area of the body.

When using this product avoid contact with the 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 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
  • Use on affected areas in place of your regular soap
  • Work up a rich lather using warm water and massage gently into affected areas
  • Rinse well

Other information

Store at room temperature

Inactive ingredients

sodium cocoyl isethionate, stearic acid, sodium stearate, water, sodium lauroyl sarcosinate, paraffin, petrolatum, sorbitol, cetearyl alcohol, propanediol, ceteareth-20, simethicone, glyceryl stearate, PEG-30 stearate, sorbic acid

Questions?

1-800-325-8232

www.vanicream.com

VANICREAM™ Z-Bar

Pyrithione Zinc 2%

Seborrheic Dermatitis & Anti-dandruff Medicated Cleansing Bar

  • Helps relieve itching, irritation, redness, flaking and scaling associated with dandruff and seborrheic dermatitis.
  • Mild and gentle
  • Non-comedogenic
  • Contains Vanicream™ Cream Base
  • Gluten-free
  • For face, hands, body & scalp

For information on our other products for sensitive skin, call 800-325-8232 or visit our website at www.vanicream.com.

Official Vanicream • vanicream

Mfr for PHARMACEUTICAL SPECIALTIES, INC., ROCHESTER, MN 55901

800-325-8232

www.vanicream.com

Made in U.S.A.

Vanicream is a trademark, or registered trademark of Pharmaceutical Specialties, Inc. in the US or other countries.

©PSI2015. All rights reserved.

NDC 45334-390-33

DERMATOLOGIST TESTED

VANICREAM™ Z-Bar

Pyrithione Zinc 2%

Seborrheic Dermatitis & Anti-dandruff Medicated Cleansing Bar

Free of dyes, fragrance, masking fragrance, lanolin, parabens, formaldehyde

for Sensitive Skin

Net Wt 3.36 oz (95 g)

Outside box

NDC 45334-390-00

DERMATOLOGIST TESTED

VANICREAM™ Z-Bar

Pyrithione Zinc 2%

Seborrheic Dermatitis & Anti-dandruff Medicated Cleansing Bar

Free of dyes, fragrance, masking fragrance, lanolin, parabens, formaldehyde

for Sensitive Skin

Net Wt 0.7 oz (20 g)

Small size box

VANICREAM Z-BAR 
pyrithione zinc soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45334-390
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PEG-30 STEARATE (UNII: 1U8KB35S20)  
SORBITOL (UNII: 506T60A25R)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PROPANEDIOL (UNII: 5965N8W85T)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
SORBIC ACID (UNII: X045WJ989B)  
WATER (UNII: 059QF0KO0R)  
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
SODIUM STEARATE (UNII: QU7E2XA9TG)  
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
PARAFFIN (UNII: I9O0E3H2ZE)  
PETROLATUM (UNII: 4T6H12BN9U)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:45334-390-331 in 1 CARTON09/19/201608/31/2022
195 g in 1 BAG; Type 0: Not a Combination Product
2NDC:45334-390-0020 g in 1 CARTON; Type 0: Not a Combination Product09/15/201610/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H09/15/201608/31/2022
Labeler - Pharmaceutical Specialties, Inc. (076499557)

Revised: 4/2021
 
Pharmaceutical Specialties, Inc.