SPF 50 Daily UV Defense Broad Spectrum Sunscreen

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
SPF 50 Daily UV Defense Broad Spectrum Sunscreen
Generic name
OCTINOXATE, ZINC OXIDE
Manufacturer
Vi Medical Products, INC
Product type
HUMAN OTC DRUG
SPL set ID
2d814f8a-23b5-209f-e063-6394a90a5091
SPL ID
37f244fd-c02e-e66a-e063-6394a90aed81
Version
3
Effective date
2025-06-19
Source export date
2026-08-01
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/d245bd7ce31d1d8ed63276109973402ece6c44860774da30f25b731cd7418983/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:34:32
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: For external use only. Avoid contact with eyes. Rinse with water to remove. Do not use on damaged or broken skin.