Daily Defense Facial Sunscreen Plus Primer

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

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

Brand name: Daily Defense Facial Sunscreen Plus Primer
Generic name: TITANIUM DIOXIDE, ZINC OXIDE
Manufacturer: LAURA CATHERINE, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 36e84147-5dcd-517a-e063-6394a90a54ee
SPL ID: 4604ffc9-70fc-d16f-e063-6294a90aa3f8
Version: 2
Effective date: 2025-12-15
Source export date: 2026-10-27
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:07:28

Harmonized routes table
Harmonized routes
TOPICAL

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Daily Defense Facial Sunscreen Plus Primer	openfda.brand_name
generic name		TITANIUM DIOXIDE, ZINC OXIDE	openfda.generic_name
manufacturer name		LAURA CATHERINE, LLC	openfda.manufacturer_name
ndc	package	85596-203-15	openfda.package_ndc
ndc	product	85596-203	openfda.product_ndc
ndc11	package	85596020315	derived:openfda.package_ndc
spl id		4604ffc9-70fc-d16f-e063-6294a90aa3f8	id
spl set id		36e84147-5dcd-517a-e063-6394a90a54ee	set_id
unii		SOI2LOH54Z	openfda.unii
unii		15FIX9V2JP	openfda.unii

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