NAKED SUNDAYS BEACH DAY ALL OVER WATER MIST

Manufacturer
WILD CHILD LABORATORIES PTY LTD
Effective date
2024-10-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:51:50

Label at a glance#

ProductNAKED SUNDAYS BEACH DAY ALL OVER WATER MIST SPF 45
Active ingredientOCTOCRYLENE, ENSULIZOLE, AVOBENZONE
Label structure10 sections

Indications and uses

Uses: Helps prevent sunburn. If used as directed with other sun protection measures (see directions), decreases the risk of skin cancer and early skin ageing caused by the sun.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Avobenzone 1.5%

Octocrylene 5%

Phenylbenzimidazole Sulfonic Acid 3%

Purpose

OTC - PURPOSE SECTION

Sunscreen

USES

INDICATIONS & USAGE SECTION

Uses: Helps prevent sunburn. If used as
directed with other sun protection measures
(see directions), decreases the risk of skin
cancer and early skin ageing caused by the sun.

WARNINGS

WARNINGS SECTION

Warnings: For external use only. Do not use
on damaged or broken skin

Keep out of eyes, Rinse with water to remove

Keep out of reach of children.
Stop use and ask a doctor if rashes occur.
If product is swallowed, get medical help or
contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • SPRAY 7 TIMES WITH MOUTH AND LIPS CLOSED 8-10" AWAY FROM FACE 15 MINUTES BEFORE SUN EXPOSURE.
  • Reapply after 80 minutes of swimming or sweating.
  • Reapply immediately after towel drying.
  • Reapply at least every 2 hours.
  • Children under 3 years 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 10.00AM - 2.00PM
  • Wear long-sleeved shirts, pants, hats, and sunglasses

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified water, Sorbitol. Pentylene glycol , Hydroxyapatite, PEG/PPG Dimethicone, Potassium Chloride, Phenoxyethanol, Citrullus lantus , Sodium Hydroxide, Hydroxyacetophenone, Microcrystalline Cellulose, Cellulose gum, Silica, Ethylhexylglycerin, PVP, Fragrance ( Natural) , Aloe Barbadensis Leaf Juice, Sodium Benzoate

OTHER INFORMATION

OTHER SAFETY INFORMATION

Other Information: Protect this product
from excess heat and direct sun. Store below
30°C / 86°F.

USER SAFETY WARNINGS SECTION

Directions: Avoid Eye Area, Shake well before use.

Use as top up sunscreen only. Hold 8-10" away from your body and spray liberally & evenly until skin feels moist 15 minutes before sun exposure. Do not spray directly on to face. Make sure no spots are missed by spraying onto hands and applying to face. DO not apply in windy conditions.

Use in well-ventilated area. Avoid inhalation. Use a water resistant sunscreen if swimming or sweating. Reapply immediately after towel drying. Reapply at least every 2 hours.

Children under 6 months of age ask a doctor

OTC - PURPOSE SECTION

Sunscreen

OTC - ASK DOCTOR SECTION

If rashes occur

OTHER SAFETY INFORMATION

Sun Protection measure

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 measure including: Limit time in the sun,especially from 10:00 AM to 02:00 PM. Wea long sleeved shirts pants hats and sunglasses

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30807-251030807-2510-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
24be3560-5c8c-9163-e063-6394a90afa8b24be442e-d2d3-b829-e063-6394a90a18022024-10-18WarningsExact identifier
spl id: 24be3560-5c8c-9163-e063-6394a90afa8b
spl set id: 24be442e-d2d3-b829-e063-6394a90a1802

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.