BONDI SANDS SPF 60 SUNNY SPRITZ FACE MIST- homosalate, octocrylene, octisalate, avobenzone aerosol, spray

Bondi Sands SPF 60 Sunny Spritz Face Mist by

Drug Labeling and Warnings

Bondi Sands SPF 60 Sunny Spritz Face Mist by is a Otc medication manufactured, distributed, or labeled by BONDI SANDS (USA) INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Avobenzone 3%

Homosalate 10.5%

Octisalate 3.5%

Octocrylene 5.6%

Purpose

Sunscreen

Uses

• Helps prevent sunburn.
• 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.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. If eye contact occurs, rinse thoroughly with clean running water.

Stop use and ask a doctor

if rash or irritation occurs.

Keep out of reach of children.

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

Flammable. Warning.

Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F. Keep out of reach of children. Use only as directed. Intentional misuse by deliberately concentrating and inhaling can be harmful or fatal.

Directions

• Shake well before use.
• Hold spray 8-10 inches away from face with eyes and mouth closed before using.
• Do not apply the product in windy conditions.
• Apply liberally and evenly 15 minutes before sun exposure.
• Use a water resistant sunscreen if swimming or sweating.
• Reapply:
• immediately after towel drying.
• at least every 2 hours.
• 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.
• Children under 6 months: Ask a doctor.

Other Information

• Protect the product in this container from excessive heat and direct sun.
• You may report a serious adverse reaction to 888-339-7642; Monday-Friday, 9 am - 5 pm.

Inactive Ingredients

Alcohol Denat., Butane, Isobutane, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Acrylates/Octylacrylamide Copolymer, Cyclopentasiloxane, Diethylhexyl 2,6-Naphthalate, Glycerin, Water/Aqua/Eau, Propane, Erythritol, Tocopheryl Acetate, Hibiscus Sabdariffa Fruit Extract

Questions?

888-339-7642 or visit bondisands.com

Product Labeling

INGREDIENTS AND APPEARANCE

BONDI SANDS SPF 60 SUNNY SPRITZ FACE MIST 
homosalate, octocrylene, octisalate, avobenzone aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79950-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	35 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	56 mg  in 1 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	105 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
BUTANE (UNII: 6LV4FOR43R)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
ERYTHRITOL (UNII: RA96B954X6)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
WATER (UNII: 059QF0KO0R)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANE (UNII: T75W9911L6)
ISOBUTANE (UNII: BXR49TP611)
ACRYLATES/OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79950-016-01	1 in 1 CARTON	01/06/2025
1		60 g in 1 CAN; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/06/2025

Labeler - BONDI SANDS (USA) INC. (117596864)