BeautyBarrier

Manufacturer
NAKED SUNDAYS PTY LTD
Effective date
2026-01-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:33:10

Label at a glance#

ProductBeautyBarrier
Active ingredientZINC OXIDE
Label structure10 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 24.5%.

Purpose

OTC - PURPOSE SECTION

Sunscreen

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Butyloctyl Salicylate, Calcium Gluconate, Caprylic/CapricTriglyceride, Centella Asiatica Leaf Extract, Cetearyl Alcohol, Cetearyl Glucoside, Citrullus Lanatus (Watermelon) Seed Oil, Coco-Caprylate/Caprate, Disodium EDTA, Ethylhexyl Methoxycrylene, Ethylhexylglycerin, Gluconolactone, Glycerin, Hydrolyzed Adansonia Digitata Seed Extract, Hydrolyzed Soy Protein, Iron Oxides (CI 77492, CI 77491, CI 77499), Isostearic Acid, L-Proline, PEG-30 Dipolyhydroxystearate, Phenoxyethanol, Polyglyceryl-3 Polyricinoleate, Rice Amino Acids, Sodium Benzoate, Sodium Chloride, Tocopherol, Water, Xanthan Gum

Other Information

OTHER SAFETY INFORMATION


Protect this product from excess heat
and direct sun.


Store below 30°C / 86°F

Questions:
info@nakedsundays.com

usage

INDICATIONS & USAGE SECTION


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.

Warning

WARNINGS SECTION

Warnings: For external use only.


Do not use on damaged or broken skin.


When using this product: Keep out of eyes. Rinse with water to remove.


Stop use and ask a doctor: If rash occurs.

Dosage

DOSAGE & ADMINISTRATION SECTION

Directions:
Apply liberally & evenly 15 minutes before sun exposure. Avoid eye area.

Reapply at least every 2 hours or immediately after swimming, sweating
or towel drying.


Use a water-resistant sunscreen if swimming or sweating.


Children under 6 months of age: Ask a Doctor

Other Safety Information

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 10AM to 2PM


Wear long-sleeved shirts, pants, hats, and sunglasses

Keep out of reach of children:

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.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11BeautyBarrier


MINERAL PERFECTING PRIMING LOTION

SPF50

with Centella Asiatica

BROAD SPECTRUM SPF 50

50ml • 1.69fl. oz.

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81104-282-02BeautyBarrier50 mL in 1 TUBELOTION501

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81104-28281104-282-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 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
BeautyBarrierZINC OXIDENAKED SUNDAYS PTY LTD45740afa-230d-4dd5-e063-6394a90a102f2026-01-15WarningsExact identifier
ndc (package): 81104-282-02
ndc (product): 81104-282
ndc11 (package): 81104028202
spl id: 45740afa-230e-4dd5-e063-6394a90a102f
spl set id: 45740afa-230d-4dd5-e063-6394a90a102f

Reported adverse events (FAERS/openFDA)#

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