VANICREAM- pyrithione zinc shampoo 
Pharmaceutical Specialties, Inc.

----------

VANICREAM™ Dandruff Shampoo

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

Other information

Store at room temperature

Inactive ingredients purified water, lauryl glucoside, coco-glucoside, acrylates copolymer, panthenol, pentylene glycol, glycerin, sucrose cocoate, disodium cocoyl glutamate, sodium cocoyl glycinate, behenyl alcohol, sucrose stearate, cetyl palmitate, sodium cocoyl glutamate, 1,2-hexanediol, sodium hydroxide, caprylyl glycol, sodium chloride

Questions?

1-800-325-8232

www.vanicream.com

Dist. by

PHARMACEUTICAL SPECIALTIES, INC.

ROCHESTER, MN 55901 • Made in U.S.A.

www.vanicream.com • 1-800-325-8232

NDC 45334-206-08

Formerly known as Free & Clear™

VANICREAM™

Pyrithione Zinc 2%

Dandruff Shampoo

for Sensitive Skin

DERMATOLOGIST TESTED

Free of dyes, fragrance, masking fragrance, lanolin, protein, parabens, & formaldehyde releasers

Sulfate-free • Betaine-free • Gluten-free

8 fl oz (237 mL)

45334-206 Dandruff Shampoo

VANICREAM 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45334-206
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (4500 MPA.S) (UNII: T967IEU43C)  
SUCROSE COCOATE (UNII: 3H18P0UK73)  
SUCROSE STEARATE (UNII: 274KW0O50M)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
COCO GLUCOSIDE (UNII: ICS790225B)  
SODIUM COCOYL GLYCINATE (UNII: XLU9KH03XM)  
WATER (UNII: 059QF0KO0R)  
DOCOSANOL (UNII: 9G1OE216XY)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
GLYCERIN (UNII: PDC6A3C0OX)  
DEXPANTHENOL (UNII: 1O6C93RI7Z)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:45334-206-08237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/03/2022
2NDC:45334-206-077.4 mL in 1 TUBE; Type 0: Not a Combination Product01/03/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03201/03/2022
Labeler - Pharmaceutical Specialties, Inc. (076499557)
Establishment
NameAddressID/FEIBusiness Operations
Pharmaceutical Specialties, Inc.076499557manufacture(45334-206)

Revised: 10/2023
Document Id: d9e02590-19a1-f0d8-e053-2a95a90a8e2a
Set id: d124a093-f739-0666-e053-2995a90a52ed
Version: 2
Effective Time: 20231002
 
Pharmaceutical Specialties, Inc.