BLUE LIZARD SENSITIVE SPF 50 SUNSCREEN- titanium dioxide and zinc oxide lotion 
Crown Laboratories

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Blue Lizard Sensitive SPF 50 Sunscreen

Active ingredients

Titanium Dioxide 8%

Zinc Oxide 10%

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

• shake well prior to use

• Apply liberally 15 minutes before sun exposure

• children under 6 months: Ask a doctor

Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: l

• reapply:

Other information

Inactive ingredients

Alumina, Aluminum Stearate, Beeswax, C12-15 Alkyl Benzoate, Caprylyl Glycol, Cetyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Chlorphenesin, Dimethicone, Disodium EDTA, Ethylhexyl Palmitate, Ethylhexyl Stearate, Hexyl Laurate, Hydrogenated Castor Oil, Methyl Glucose Dioleate, Octyldodecyl Neopentanoate, PEG-7 Hydrogenated Castor Oil, Phenoxyethanol, Polyglyceryl-4 Isostearate, Polyhydroxystearic Acid, Propanediol, Purified Water, Sorbitan Oleate, Stearic Acid, Tocopheryl Acetate (Vitamin E), Triethoxycaprylylsilane, Trimethylsiloxysilicate, VP Hexadecene Copolymer

Questions?

Call 800.877.8869 or visit www.bluelizardsunscreen.com

Crown Laboratories, Inc., Johnson City, TN 37604

Blue Lizard Sensitive 3oz Tube

BLUE LIZARD

AUSTRALIAN SUNSCREEN

50+

UVA/UVB PROTECTION

BROAD SPECTRUM SPF 50+

TRUSTED BY DERMATOLOGISTS FOR OVER 20 YEARS

SENSITIVE

mineral sunscreen

Smart Cap TECHNOLOGY

CAP CHANGES COLOR IN HARMFUL UV LIGHT

WATER RESISTANT (80 MINUTES)

3fl oz (89ml)

P11661.03

BL Sensitive SPF 50 P11661_03

BLUE LIZARD SENSITIVE SPF 50 SUNSCREEN 
titanium dioxide and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-2046
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE89.6 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE112 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PEG-7 HYDROGENATED CASTOR OIL (UNII: WE09129TH5)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
PROPANEDIOL (UNII: 5965N8W85T)  
WATER (UNII: 059QF0KO0R)  
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
HEXADECYL POVIDONE (4 HEXADECYL BRANCHES/REPEAT) (UNII: AG75W62QYU)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRIMETHYLSILOXYSILICATE (M/Q 0.8-1.0) (UNII: 25LXE464L2)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
ALUMINUM STEARATE (UNII: U6XF9NP8HM)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
ETHYLHEXYL PALMITATE (UNII: 2865993309)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
HEXYL LAURATE (UNII: 4CG9F9W01Q)  
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
METHYL GLUCOSE DIOLEATE (UNII: FA9KFJ4Z6P)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-2046-105 mL in 1 PACKET; Type 0: Not a Combination Product03/02/2020
2NDC:0316-2046-3089 mL in 1 TUBE; Type 0: Not a Combination Product02/17/2020
3NDC:0316-2046-40148 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/29/2020
4NDC:0316-2046-50259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/24/2020
5NDC:0316-2046-45148 mL in 1 TUBE; Type 0: Not a Combination Product02/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/29/2020
Labeler - Crown Laboratories (079035945)
Establishment
NameAddressID/FEIBusiness Operations
Crown Laboratories079035945manufacture(0316-2046)

Revised: 12/2023
Document Id: 0bc74f51-ac53-4b1b-e063-6294a90a6d30
Set id: 9d20b230-2cce-4d90-e053-2995a90a4c03
Version: 4
Effective Time: 20231205
 
Crown Laboratories