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

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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Blue Lizard Sensitive Face Sunscreen

Active Ingredients

Titanium Dioxide 1.0%

Zinc Oxide 7.8%

Purpose

Sunscreen

Uses

Warnings

Directions

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 TURNS BLUE IN HARMFUL UV LIGHT

WITH HYDRATING HYALURONIC ACID

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 not finalpart35201/30/2019
Labeler - Crown Laboratories (079035945)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories079035945manufacture(0316-2056)

Revised: 10/2021
Document Id: ce40ce5a-0706-8ce8-e053-2a95a90af833
Set id: 88dbd396-8955-271e-e053-2995a90a0a7a
Version: 2
Effective Time: 20211013
 
Crown Laboratories