FDA.reportPublic FDA data

RE SCREEN BROAD SPECTRUM SPF 30 SUNSCREEN STICK

Manufacturer
Zouck LLC
Effective date
2026-04-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:55:19

Label at a glance#

ProductRE SCREEN BROAD SPECTRUM SPF 30 SUNSCREEN
Active ingredientZINC OXIDE
Label structure12 sections

Storage and handling

Other information Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 18%

OTC - PURPOSE SECTION

Sunscreen

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.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor If rash occurs

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.

DOSAGE & ADMINISTRATION SECTION

Directions Apply liberally 15 minutes
before sun exposure Reapply after 80
minutes of swimming or sweating
immediately after towel drying at least
every 2 hours Children under 6 months:
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: (cont.)

INACTIVE INGREDIENT SECTION

Olea Europaea (Olive) Oil, Beeswax, Simmondsia
Chinensis (Jojoba) Seed Oil,
Theobroma Cacao (Cocoa)
Seed Butter, Butyrospermum
Parkii (Shea) Butter,Tocopheryl Acetate

STORAGE AND HANDLING SECTION

Other information
Protect this product from
excessive heat and direct sun.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelingLabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87608-001-01RE SCREEN BROAD SPECTRUM SPF 30 SUNSCREEN1 g in 1 CONTAINERSTICK11
87608-001-02RE SCREEN BROAD SPECTRUM SPF 30 SUNSCREEN1 in 1 BOXSTICK11

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87608-00187608-001-01, 87608-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
ZINC OXIDESOI2LOH54ZACTIB
THEOBROMA CACAO (COCOA) SEED BUTTER512OYT1CRRIACT
BEESWAX2ZA36H0S2VIACT

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
RE SCREEN BROAD SPECTRUM SPF 30 SUNSCREENZINC OXIDEZouck LLC507560fe-c7ad-329a-e063-6394a90a039a2026-04-27WarningsExact identifier
ndc (package): 87608-001-01
ndc (package): 87608-001-02
ndc (product): 87608-001
ndc11 (package): 87608000101
ndc11 (package): 87608000102
spl id: 507560fe-c7ae-329a-e063-6394a90a039a
spl set id: 507560fe-c7ad-329a-e063-6394a90a039a

Reported adverse events (FAERS/openFDA)#

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