Bondi Sands Sunny Daze Hydrating Broad Spectrum Sunscreen SPF 50 Lotion

Bondi Sands Sunny Daze Hydrating Broad Spectrum Sunscreen SPF 50 by

Drug Labeling and Warnings

Bondi Sands Sunny Daze Hydrating Broad Spectrum Sunscreen SPF 50 by is a Otc medication manufactured, distributed, or labeled by Baxter Laboratories Pty. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BONDI SANDS SUNNY DAZE HYDRATING BROAD SPECTRUM SUNSCREEN SPF 50- zinc oxide lotion 
Baxter Laboratories Pty. Ltd.

----------

Bondi Sands Sunny Daze Hydrating Broad Spectrum Sunscreen SPF 50 Lotion

Active Ingredients

Zinc Oxide 25%

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.

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.

When using this product

keep out of eyes. Rinse with water to remove.

Directions

  • Apply liberally 15 minutes before sun exposure.
  • Reapply:
  • Every 2 hours
  • Use a water resistant sunscreen if swimming or sweating.
  • 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 888-266-0772; Monday – Friday, 9 am – 5 pm.

Inactive Ingredients

Water, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Glycerin, Polyhydroxystearic Acid, Cetearyl Alcohol, Phenoxyethanol, Polyurethane-62, Benzyl Alcohol, Saccharide Isomerate, Citric Acid, Propanediol, Lecithin, Xanthan Gum, Sodium Phytate, Ethylhexylglycerin, Trideceth-6, Tocopherol, Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Sodium Citrate, Erythritol, Hibiscus Sabdariffa Fruit Extract, Iron Oxides.

Questions?

888-266-0772 or visit bondisands.com

Product Packaging

bondi sands

Everyday skincare

Sunny

Daze

HYDRATING

BROAD SPECTRUM

SUNSCREEN SPF 50

+ HIBISCUS FRUIT EXTRACT

Australian Made

1.76 OZ. (50g)

sunny daze

BONDI SANDS SUNNY DAZE HYDRATING BROAD SPECTRUM SUNSCREEN SPF 50 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70157-020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE250 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ERYTHRITOL (UNII: RA96B954X6)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
HIBISCUS SABDARIFFA WHOLE (UNII: UH3Z91Y49Y)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
PROPANEDIOL (UNII: 5965N8W85T)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
WATER (UNII: 059QF0KO0R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
TOCOPHEROL (UNII: R0ZB2556P8)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
GLYCERIN (UNII: PDC6A3C0OX)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
POLYURETHANE-62 (UNII: TBK645J3J8)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70157-020-011 in 1 CARTON08/25/202110/01/2024
150 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02008/25/202110/01/2024
Labeler - Baxter Laboratories Pty. Ltd. (740537709)

Revised: 10/2025