VANICREAM SUNSCREEN BROAD SPECTRUM SPF 50- zinc oxide cream 
Pharmaceutical Specialties, Inc.

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VANICREAM Sunscreen BROAD SPECTRUM SPF 50+

Drug Facts

Active ingredient

Zinc oxide 12%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information protect this product from excessive heat and direct sun

Inactive ingredients allantoin, butyloctyl salicylate, C12-15 alkyl benzoate, caprylyl glycol, dimethiconol/propylsilsesquioxane/silicate crosspolymer, glyceryl behenate, glyceryl dibehenate, glyceryl stearate, isodecyl salicylate, isopropyl isostearate, lecithin, neopentyl glycol diheptanoate, 1,2-hexanediol, polyester-7, polyglyceryl-3 polyricinoleate, propanediol, silica silylate, sodium chloride, squalane, tribehenin, tridecyl salicylate, water

Questions or Comments?

1-800-325-8232

www.vanicream.com

Vanicream is a trademark, or registered trademark of Pharmaceutical Specialties, Inc. in the U.S. or other countries. ©PSI 2020. All rights reserved.

Dist. by

PHARMACEUTICAL SPECIALTIES, INC.

ROCHESTER, MN 55901 Made in USA

NDC 45334-332-03

DERMATOLOGIST TESTED

New Formula

VANICREAM™ Sunscreen

BROAD SPECTRUM SPF 50+

MINERAL SUNSCREEN

WATER RESISTANT (80 MINUTES)

NON-COMEDOGENIC

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

Gluten-Free

for Sensitive Skin

Net Wt 3 oz (85 g)

Vanicream Sunscreen Broad Spectrum SPF50+

VANICREAM SUNSCREEN BROAD SPECTRUM SPF 50 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45334-332
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE12 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)  
ALLANTOIN (UNII: 344S277G0Z)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB)  
GLYCERYL MONOBEHENATE (UNII: A626UU0W2A)  
GLYCERYL 1,3-DIBEHENATE (UNII: 84T2X52XS0)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISODECYL SALICYLATE (UNII: S7097PFP4C)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
WATER (UNII: 059QF0KO0R)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
POLYESTER-7 (UNII: 0841698D2F)  
SQUALANE (UNII: GW89575KF9)  
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)  
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)  
PROPANEDIOL (UNII: 5965N8W85T)  
SILICA, TRIMETHYLSILYL CAPPED (UNII: VU10KU4B9S)  
TRIBEHENIN (UNII: 8OC9U7TQZ0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:45334-332-031 in 1 CARTON04/05/2021
185 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02004/05/2021
Labeler - Pharmaceutical Specialties, Inc. (076499557)

Revised: 10/2023
Document Id: 08677f2c-1457-86e9-e063-6394a90ac784
Set id: b5597ee1-9f82-702e-e053-2a95a90aaa7b
Version: 3
Effective Time: 20231023
 
Pharmaceutical Specialties, Inc.