SHIELD- zinc oxide cream 
Bellus Medical, LLC

----------

Zinc Oxide 21%

Sunscreen

For external use only. Do not use on damaged or broken skin. Stop use and ask doctor if rash and irritation develops and lasts.

Avoid contact with eyes if product gets into eyes rinse thoroughly with water.

If swallowed get medical help or contact poison control center right away.

Evenly apply to skin before
exposure to sun and as needed.
• Children under 6 months,
ask doctor.
• Protect this product from
excessive heat and direct sun.

Argania Spinosa Kernel Oil, Caprylic/
Capric Triglyceride, Cetearyl
Alcohol, Cetearyl Glucoside,Cetearyl
Olivate, Coco-Caprylate/-
Caprate , Cocoglycerides, Coconut
Alkanes , Copernicia Cerifera
(Carnauba) Wax, Diethylhexanoate,
Ethyl Macadamiate, Glycerin, Glyceryl
Caprylate, Glyceryl Isostearate,
Glyceryl Undecylenate, Iron
Oxides, Lysolecithin, Neopentyl
Glycol, p-Anisic acid, Polyglyceryl-3
Polyricinoleate, Polyglyceryl-3
Stearate, Polyhydroxystearic Acid,
Potassium Cetyl Phosphate, Propanediol,
Simmondsia Chinensis
(Jojoba) Seed Oil, Sodium Chloride,
Sorbitan Olivate, Tocopherol Linoleate
/ Oleate, Triethoxycaprylylsilane,
Water (Aqua), Xanthan Gum.

Keep out of reach of children.

Call 888.372.3982

Distributed by: Crown Aesthetics

Dallas, TX 75244

All registered trademarks belong to Crown Aesthetics.

Helps prevent sunburn and photodamage caused by UVA/UVB exposure
Higher SPF gives more sunburn protection
If used as directed with other sun protection measures (see DIRECTIONS), decreases the risks of skin cancer and early skin aging caused by the sun

SF_30ml_Box_SHIELD_FINAL_v3_160321 JPEG_Page_1

SHIELD 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71888-104
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE21 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
COCONUT ALKANES (UNII: 1E5KJY107T)  
PROPANEDIOL (UNII: 5965N8W85T)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
TRICAPRYLIN (UNII: 6P92858988)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ARGAN OIL (UNII: 4V59G5UW9X)  
GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)  
COCO-CAPRYLATE (UNII: 4828G836N6)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
WATER (UNII: 059QF0KO0R)  
ETHYL MACADAMIATE (UNII: ANA2NCS6V1)  
GLYCERIN (UNII: PDC6A3C0OX)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
JOJOBA OIL (UNII: 724GKU717M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71888-104-0130 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02005/01/2015
Labeler - Bellus Medical, LLC (005677967)
Registrant - Bellus Medical, LLC (005677967)

Revised: 5/2023
Document Id: fb35ff9c-6ea6-474a-e053-6394a90ab4cb
Set id: 60530049-b2b8-3ad6-e053-2991aa0aff80
Version: 2
Effective Time: 20230508
 
Bellus Medical, LLC