Solarium Daily Essentials Luminizing Glow Drops

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: Solarium Daily Essentials Luminizing Glow Drops
Generic name: ZINC OXIDE
Manufacturer: Solarium Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: 302a4efe-d429-b1c4-e063-6294a90a073d
SPL ID: 43cc8ed8-24ef-87bb-e063-6394a90a5f8f
Version: 3
Effective date: 2025-11-17
Source export date: 2026-10-27
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:05:35

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Solarium Daily Essentials Luminizing Glow Drops	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		Solarium Brands LLC	openfda.manufacturer_name
ndc	package	84891-2191-1	openfda.package_ndc
ndc	product	84891-2191	openfda.product_ndc
ndc11	package	84891219101	derived:openfda.package_ndc
spl id		43cc8ed8-24ef-87bb-e063-6394a90a5f8f	id
spl set id		302a4efe-d429-b1c4-e063-6294a90a073d	set_id
unii		SOI2LOH54Z	openfda.unii

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

Warnings sections page 1 of 1 · 1 matching rows.

Solarium Daily Essentials Luminizing Glow Drops Warning Label

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