BONDI SANDS FRAGRANCE FREE FACE SPF 50 SUNSCREEN- 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 Fragrance Free Face SPF 50 Sunscreen Lotion

Drug Facts

Active Ingredients

Avobenzone 3%, Homosalate 10%, Octisalate 5%, Octocrylene 8%

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/Aqua/Eau, Beeswax/Cera Alba/Cire d'abeille, Aloe Barbadensis Leaf Juice, Isopropyl Palmitate, Cetearyl Alcohol, Cyclopentasiloxane, Cyclohexasiloxane, Ceteareth-20, Hydroxyacetophenone, Carbomer, Benzyl Alcohol, Saccharide Isomerate, Phenoxyethanol, Sodium Stearoyl Glutamate, Triethanolamine, Tocopheryl Acetate, Sodium Chloride, Citric Acid.

Questions?

888-266-0772 or visit bondisands.com

Company Information

Made in Australia.

Distributed by Bondi Sands USA

Wilmingon, 19808, DE.

bondisands.com

Product Packaging

bondi sands

The Australian tan

DAILY MOISTURIZING

FACE

SPF 50

BROAD SPECTRUM

VERY WATER RESISTANT 80 MINUTES

FRAGRANCE FREE

SUNSCREEN LOTION

REEF FRIENDLY

72HR HYDRATION

SUITABLE FOR SENSITIVE SKIN

Australian Made

2.53 FL. OZ. (75mL)

face spf50

BONDI SANDS FRAGRANCE FREE FACE SPF 50 SUNSCREEN 
avobenzone, homosalate, octisalate, octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79950-006
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) OCTOCRYLENE80 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
TROLAMINE (UNII: 9O3K93S3TK)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79950-006-0175 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/01/2021
Labeler - BONDI SANDS (USA) INC. (117596864)

Revised: 8/2020
Document Id: acda9863-ad9e-e430-e053-2995a90a69a6
Set id: acda9863-ad9f-e430-e053-2995a90a69a6
Version: 1
Effective Time: 20200814
 
BONDI SANDS (USA) INC.