NAKED SUNDAYS GLOW BODY MIST SUNSCREEN SPRAY SPF 50 +

Manufacturer
NAKED SUNDAYS PTY LTD
Effective date
2025-03-23
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:58:20

Label at a glance#

ProductGLOW BODY MIST SPF 50
Active ingredientOCTOCRYLENE, AVOBENZONE, HOMOSALATE, OCTISALATE
Label structure12 sections

Dosage and administration

Generously spray to exposed areas holding bottle 10-15 cm away from skin. Ensure even application by spraying at least 7 times per section of body until product is visible, Rub in lightly. Use a water- resistant sunscreen if swimming or sweating. reapply at least every 2 hours. Children under 6 months of age : ask a doctor

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE 3% SUNSCREEN

HOMOSALATE 10% SUNSCREEN

OCTISALATE 5 % SUNSCREEN

OCTOCRYLENR 8 % SUNSCREEN

USE

INDICATIONS & USAGE SECTION

Helps prevent Sunburn

If used as directed with other sun Protection measure ( see directions), decrease the risk of skin cancer and early skin ageing caused by the sun

warning

WARNINGS SECTION

For External use Only

Do not use on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

Keep out of eyes, Rinse with water to remove

stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs

Keep Out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if Product is swallowed , get medical help or contact a poison control center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Generously spray to exposed areas holding bottle 10-15 cm away from skin. Ensure even application by spraying at least 7 times per section of body until product is visible, Rub in lightly.

Use a water- resistant sunscreen if swimming or sweating.

reapply at least every 2 hours.

Children under 6 months of age : ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

alcohol, Citrullius Lanatus Seed oil, Kakadu Plum, Tocopheryl Acetate, Fragrance

other information

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat & direct sun

Sun Protection Measures

SUMMARY OF SAFETY AND EFFECTIVENESS

Spending time in the Sun Increases your risk of skin cancer and early skin ageing. 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 10.00 AM - 2.00 PM

Wea long-sleeved Shirts , pants hats, and sunglasses,

OTC - PURPOSE SECTION

Sunscreen

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81104-110-01GLOW BODY MISTSPF 50150 mL in 1 BOTTLE, SPRAYSPRAY1506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81104-110GLOW BODY MIST SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) SPRAY [NAKED SUNDAYS PTY LTD]6Current NDC, Legacy NDC, 1 package rows20250402_cba78484-3c0b-413e-e053-2995a90aad86.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81104-11081104-110-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
GLOW BODY MIST SPF 50AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENENAKED SUNDAYS PTY LTDcba78484-3c0b-413e-e053-2995a90aad862025-03-23WarningsExact identifier
ndc (package): 81104-110-01
ndc (product): 81104-110
ndc11 (package): 81104011001
spl id: 3104ef25-5074-942d-e063-6394a90aec24
spl set id: cba78484-3c0b-413e-e053-2995a90aad86

Reported adverse events (FAERS/openFDA)#

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