SunDrops 87

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: SunDrops 87
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Sunburst Chemicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 584ea129-aaf2-402f-b9f1-3fec2a23a21c
SPL ID: 435389b8-9dde-0d17-e063-6294a90ab9b8
Version: 8
Effective date: 2025-11-11
Source export date: 2026-10-30
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/8d15bdc5962e7531569eaeb5b1b2e4919574d40a6782ab67345a27b890175a00/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:58:27

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		SunDrops 87	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Sunburst Chemicals, Inc.	openfda.manufacturer_name
ndc	package	63621-387-50	openfda.package_ndc
ndc	package	63621-387-65	openfda.package_ndc
ndc	package	63621-387-40	openfda.package_ndc
ndc	package	63621-387-14	openfda.package_ndc
ndc	product	63621-387	openfda.product_ndc
ndc11	package	63621038765	derived:openfda.package_ndc
ndc11	package	63621038740	derived:openfda.package_ndc
ndc11	package	63621038750	derived:openfda.package_ndc
ndc11	package	63621038714	derived:openfda.package_ndc
rxcui		1233282	openfda.rxcui
spl id		435389b8-9dde-0d17-e063-6294a90ab9b8	id
spl set id		584ea129-aaf2-402f-b9f1-3fec2a23a21c	set_id
unii		F5UM2KM3W7	openfda.unii

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. When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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