BLUE LIZARD SENSITIVE FACE SUNSCREEN- titanium dioxide, zinc oxide gel 
Crown Laboratories

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Blue Lizard Sensitive Face Sunscreen

Active Ingredients

Titanium Dioxide 1.0%

Zinc Oxide 7.8%

Purpose

Sunscreen

Uses

Warnings

Directions

Keep out of reach of children

Other Information

Inactive Ingredients

Alumina, Aluminum Stearate, Beeswax, C12-15 Alkyl Benzoate, C13-14 Isoparaffin, Caffeine, Camellia Sinensis Leaf (Green Tea) Extract, Caprylyl Glycol, Chlorphenesin, Cyclomethicone, Dimethoxydiphenylsilane, Isostearyl Alcohol, Laureth-7, Lauryl PEG/PPG 18/18 Methicone, Phenoxyethanol, Polyacrylamide, Polyhydroxystearic Acid, Purified Water, Sodium Hyaluronate, Triethoxycaprylylsilane

Questions?

Visit www.bluelizardsunscreen.com or call 800.877.8869

Crown Laboratories, Inc., Johnson City, TN 37604

Blue Lizard Sensitive Face Tube

BLUE LIZARD

AUSTRALIAN SUNSCREEN

30+

UVA/UVB PROTECTION

BROAD SPECTRUM

SPF 30+

TRUSTED BY DERMATOLOGISTS FOR OVER 20 YEARS

SENSITIVE face

mineral sunscreen

Smart Cap TECHNOLOGY

CAP CHANGES COLOR IN HARMFUL UV LIGHT

WITH HYDRATING HYALURONIC ACID

Mineral Sunscreen

Protects your skin by acting like thousands of tiny shields that reflect UV rays.

P11467.02

p1146702

Blue Lizard Sensitive Face Carton

P11468.02

p1146802

BLUE LIZARD SENSITIVE FACE SUNSCREEN 
titanium dioxide, zinc oxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-2056
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE83.4 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CYCLOMETHICONE (UNII: NMQ347994Z)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
LAURETH-7 (UNII: Z95S6G8201)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
CAFFEINE (UNII: 3G6A5W338E)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)  
ALUMINUM STEARATE (UNII: U6XF9NP8HM)  
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)  
DIMETHOXYDIPHENYLSILANE (UNII: 02QB6788GC)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-2056-171 in 1 CARTON01/30/2019
148 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/30/2019
Labeler - Crown Laboratories (079035945)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories079035945manufacture(0316-2056)

Revised: 12/2023
Document Id: 0bc550a7-098f-75e4-e063-6294a90a9fc1
Set id: 88dbd396-8955-271e-e053-2995a90a0a7a
Version: 4
Effective Time: 20231205
 
Crown Laboratories