ATTITUDE Sunly Kids Mineral sunscreen Spray SPF 50 Watermelon & coco

Manufacturer
9055-7588 Québec Inc.DBA ATTITUDE
Effective date
2025-11-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:22:59

Label at a glance#

ProductATTITUDE Sunly Kids Mineral sunscreen Sprayer SPF 50 Watermelon and coco
Active ingredientZINC OXIDE
Label structure10 sections

Storage and handling

Store at temperatures < 90F and protect from direct sun.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

OTC - ACTIVE INGREDIENT SECTION

Zinc oxide (24 %)

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - STOP USE SECTION

Stop use and consult a doctor if rash occurs

DOSAGE & ADMINISTRATION SECTION

Adultds and children older than 6 months • Spray liberally and spread evenly by hand 15 min before sun exposure. Hold container 4 to 6 inch/10 to 15 cm from the skin to apply. Do not spray directly onto face. Spray on hands then apply to face. Do not apply in windy conditions. Use in a well-ventilated area. Avoid inhaling or exposing others to spray. Reapply at least every 2 h or after 80 min of swimming/sweating or immediately after towel drying. • 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 ≥ 15 and other sun protection measures including: limit time in the sun, especially from 10am-2pm; and wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months of age: Ask a doctor.

INACTIVE INGREDIENT SECTION

Ethyl Oleate, Cocoglycerides, Caprylic/Capric Triglyceride, Butylene Glycol Dicaprylate/Dicaprate, Isocetyl Stearoyl Stearate, Calcium Aluminum Borosilicate, Capryloyl Glycerin/Sebacic Acid Copolymer, Hydrogenated Castor Oil/Sebacic Acid Copolymer, Polyhydroxystearic Acid, Cetearyl Olivate, Sorbitan Olivate, Helianthus Annuus (Sunflower) Seed Oil, Tocopherol, Dimethyl Heptenal*, Hexyl Acetate*, Methyldihydrojasmonate*, Linalyl Acetate*, Vanillin*, *Fragrance (Parfum).

STORAGE AND HANDLING SECTION

Store at temperatures < 90F and protect from direct sun.

OTC - QUESTIONS SECTION

Questions ? 1-855-509-7225

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ATTITUDE

EWG Verified

VEGAN

SPF 50+

UVA ¦ UVB

NON NANO

water melon & coco

mineral sunscreen

Broad spectrum SPF 50+

80min water resistant spray

kids

sunly

85g / 3 oz. net wt.

NPN 80142223

Made in Canada

Dermatologically tested

Shake

16537-0116537-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61649-537-01ATTITUDE Sunly Kids Mineral sunscreen Sprayer SPF 50 Watermelon and coco85 g in 1 TUBESPRAY851

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61649-53761649-537-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
ATTITUDE Sunly Kids Mineral sunscreen Sprayer SPF 50 Watermelon and cocoZINC OXIDE9055-7588 Qubec Inc.DBA ATTITUDE44aa1349-e3f1-9b80-e063-6294a90a0fbd2025-11-28WarningsExact identifier
ndc (package): 61649-537-01
ndc (product): 61649-537
ndc11 (package): 61649053701
spl id: 44aa0b6f-0ce3-99cd-e063-6294a90a5c99
spl set id: 44aa1349-e3f1-9b80-e063-6294a90a0fbd

Reported adverse events (FAERS/openFDA)#

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