BLUE LIZARD ACTIVE SPF 50- zinc oxide spray

Blue Lizard Active SPF 50 by

Drug Labeling and Warnings

Blue Lizard Active SPF 50 by is a Otc medication manufactured, distributed, or labeled by Crown Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Zinc Oxide 24%

Purpose

Sunscreen

Uses

• 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 risk of skin cancer and early skin aging caused by the sun.

Warnings

For external use only. Contents under pressure. Do not puncture or incinerate.

Flammable: Keep away from fire or flame.

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

Stop use and ask doctor if Rash or irritation occurs

Do not use On damaged or broken skin If allergic to any ingredient

If swallowed, get medical help or contact a Poison Control Center

Directions

Shake well prior to use.

Apply liberally to dry skin 15 minutes before sun exposure

Hold container 4 to 6 inches from the skin to apply. Rub in. Do not spray directly into face. Spray on hands then apply to face. Rub in.

Do not apply in windy conditions. Use in well-ventilated area and avoid inhalation.

For topical use only Children under 6 months of age: 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: Limit time in the sun especially from 10 a.m.- 2 p.m.

Wear long-sleeved shirts, pants, hats, and sunglasses

Reapply to dry skin: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours

Keep out of reach of children

Other Information

• Protect the product in this container from excessive heat and direct sun
• May stain some fabrics

Inactive Ingredients

Butyloctyl Salicylate, C9-12 Alkane, Caprylic/Capric Triglyceride, Caprylyl Glycol, Diisopropyl Adipate, Dimethicone Crosspolymer-3, Di-PPG-3 Myristyl Ether Adipate, Dunaliella Salina Extract, Ethylhexyl Palmitate, Fragrance, Haematococcus Pluvialis Extract, Phenoxyethanol, Polyhydroxystearic Acid, Pongamia Glabra Seed Oil, Quaternium-90 Montmorillonite, Quaternium-90 Sepiolite, Tetrafluoropropene, Triethoxycaprylylsilane

Questions?

Visit www.bluelizardsunscreen.com or call 800.877.8869

Distributed by Crown Laboratories, Inc., Johnson City, TN 37604

DOT 2Q M5706

Blue Lizard Active SPF 50+ Spray 5 oz Label

TRUSTED BY DERMATOLOGISTS FOR OVER 20 YEARS

BLUE LIZARD

AUSTRALIAN SUNSCREEN

50+

UVA/UVB PROTECTION

BROAD SPECTRUM SPF 50+

Water Resistant (80 Minutes)

ACTIVE

tropical scent

mineral sunscreen spray

100% Mineral Active Ingredient

Made with Earth Friendly Propellant

P11906.01

INGREDIENTS AND APPEARANCE

BLUE LIZARD ACTIVE SPF 50 
zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0316-2082
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	24 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DI-PPG-3 MYRISTYL ETHER ADIPATE (UNII: T32481VTXW)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
KARUM SEED OIL (UNII: 62160PU6FJ)
DUNALIELLA SALINA (UNII: F4O1DKI9A6)
HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
DODECANE (UNII: 11A386X1QH)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
1,3,3,3-TETRAFLUOROPROPENE, (1E)- (UNII: 5I2481UOO8)
QUATERNIUM-90 MONTMORILLONITE (UNII: 7BL4KVZ54U)
QUATERNIUM-90 SEPIOLITE (UNII: J9ULC97SE5)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0316-2082-05	142 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/29/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	03/29/2021

Labeler - Crown Laboratories (079035945)

Registrant - Crown Laboratories (079035945)