BONDI SANDS BROAD SPECTRUM HYDRA UV PROTECT SPF 70 FACE FLUID- avobenzone, homosalate, octisalate, octocrylene lotion 
BONDI SANDS (USA) INC.

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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BONDI SANDS BROAD SPECTRUM HYDRA UV PROTECT SPF 70 FACE FLUID

Drug Facts

Active Ingredients

Avobenzone 3%, Homosalate 12%, Octisalate 5%, Octocrylene 10%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use

on damaged or broken skin.

Keep out of reach of children.

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

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

if rash or irritation develops and lasts.

Directions

Other information

Inactive Ingredients

Water, Beeswax, C12-15 Alkyl Benzoate, Silica, PEG-15 Cocamine, Caprylyl Glycol, PEG-40 Stearate, Acrylates/Steareth-20 Methacrylate Copolymer, Caprylhydroxamic Acid, Glycerin, Carbomer, Aminomethyl Propanol, Phenoxyethanol, Sodium Carrageenan, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Sodium Chloride.

Questions?

888-266-0772 or visit bondisands.com

Company Information

Made in Australia.

Distributed by Bondi Sands USA

Wilmington, DE 19808

Product Packaging

bondi sands

The Australian tan

BROAD SPECTRUM

HYDRA

UV PROTECT

SPF 70

FACE FLUID

ULTRA LIGHTWEIGHT SUNSCREEN

PLANT BASED HYDRATION

DERMATOLOGICALLY TESTED

Australian Made

1.35 FL. OZ. (40 mL)

hydra fluid

BONDI SANDS BROAD SPECTRUM HYDRA UV PROTECT SPF 70 FACE FLUID 
avobenzone, homosalate, octisalate, octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79950-013
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE120 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PEG-15 COCAMINE (UNII: 8L6LB12TSJ)  
CARRAGEENAN (UNII: 5C69YCD2YJ)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)  
PEG-40 STEARATE (UNII: ECU18C66Q7)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79950-013-011 in 1 CARTON08/10/2021
140 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35208/10/2021
Labeler - BONDI SANDS (USA) INC. (117596864)

Revised: 8/2021
Document Id: c934db99-66c0-980c-e053-2995a90a1e56
Set id: c934db99-66c1-980c-e053-2995a90a1e56
Version: 1
Effective Time: 20210810
 
BONDI SANDS (USA) INC.