Utu Broad Spectrum SPF 50 Tinted Sunscreen-Stick - Utu Co | Filltech USA, LLC

Manufacturer
Utu Co | Filltech USA, LLC
Effective date
2026-08-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-28 00:02:03

Label at a glance#

ProductUtu Broad Spectrum SPF 50 Tinted Sunscreen-Stick
Active ingredientZINC OXIDE
Label structure7 sections

Indications and 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.

Dosage and administration

Apply liberally and evenly 15 minutes before sun exposure. Reapply after 80 minutes of swimming or sweating. Immediately after towel drying. At least every 2 hours. 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: Lim...

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

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 aging caused by the sun.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally and evenly 15 minutes before sun exposure.
Reapply after 80 minutes of swimming or sweating.
Immediately after towel drying.
At least every 2 hours.
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-2pm.
Wear long-sleeved shirts, pants, hats, sunglasses.

Warnings

WARNINGS SECTION

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.

Keep Out of Reach of Children

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ascorbic Acid, Butyloctyl Salicylate, Cera Alba, Cocos Nucifera (Coconut) Oil, Copernicia Cerifera (Carnauba) Wax, Curcuma Longa (Turmeric) Root Extract, Ethylhexyl Methoxycrylene, Helianthus Annuus (Sunflower) Seed Oil, Hydrogenated Castor Oil, Iron Oxides (CI77491), Iron Oxides (CI77492), Iron Oxides (CI77499), Mica, Ricinus Communis (Castor) Seed Oil, Sesamum Indicum (Sesame) Seed Oil, Silica, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Hyaluronate, Theobroma Cacao (Cocoa) Seed Butter, Tocopherol, Tocopheryl Linoleate / Oleate, Triethoxycaprylylsilane, Vegetable Oil.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Utu Broad Spectrum SPF 50 Tinted Sunscreen-Stick outer carton labelingUtu Broad Spectrum SPF 50 Tinted Sunscreen-Stick outer carton labelingUtu
Outdoor Skincare™
Broad Spectrum SPF 50
Tinted Sunscreen-Stick
Mineral Zinc Oxide
Water resistant 80min

Organic coconut oil, organic jojoba oil, sesame seed oil, cocoa butter, vitamin C&E.

1oz/28g

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87952-00187952-001-01, 87952-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
Utu Broad Spectrum SPF 50 Tinted Sunscreen-StickZINC OXIDEUtu Co596e17d3-3064-1cda-e063-6294a90af9632026-08-19WarningsExact identifier
ndc (package): 87952-001-01
ndc (package): 87952-001-02
ndc (product): 87952-001
ndc11 (package): 87952000102
ndc11 (package): 87952000101
spl id: 596e17d3-3065-1cda-e063-6294a90af963
spl set id: 596e17d3-3064-1cda-e063-6294a90af963

Reported adverse events (FAERS/openFDA)#

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