Zinc Oxide Perfecting Sunscreen SPF 27

Manufacturer
Epicuren Discovery
Effective date
2026-07-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-18 05:10:21

Label at a glance#

ProductZinc Oxide Perfecting Sunscreen
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTHER SAFETY INFORMATION

Other Safety InformationOther Safety Information

WARNINGS SECTION

Other informationOther information

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

INACTIVE INGREDIENT SECTION

Inactive IngInactive Ing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of ChildrenKeep Out of Reach of Children

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

INDICATIONS & USAGE SECTION

Indication and UseIndication and Use

OTC - PURPOSE SECTION

OTC PurposeOTC Purpose

Front Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84378-10084378-100-74

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-07-29full-release2026-06-01 01:08:49

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
Zinc Oxide Perfecting SunscreenZINC OXIDEEpicuren Discovery1a0228f9-bf3f-a1fe-e063-6294a90a3fb52026-07-14WarningsExact identifier
ndc (package): 84378-100-74
ndc (product): 84378-100
ndc11 (package): 84378010074
spl id: 5696f277-20b6-90e1-e063-6294a90a626b
spl set id: 1a0228f9-bf3f-a1fe-e063-6294a90a3fb5

Reported adverse events (FAERS/openFDA)#

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