SunDrops 75

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 75
Generic name: ALCOHOL
Manufacturer: Sunburst Chemicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b0623424-939e-4b49-aa99-c1ef22cf0f2d
SPL ID: 435330fc-c021-151b-e063-6394a90a229b
Version: 10
Effective date: 2025-11-11
Source export date: 2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:34:28

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		SunDrops 75	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Sunburst Chemicals, Inc.	openfda.manufacturer_name
ndc	package	63621-356-40	openfda.package_ndc
ndc	package	63621-356-50	openfda.package_ndc
ndc	package	63621-356-20	openfda.package_ndc
ndc	package	63621-356-14	openfda.package_ndc
ndc	package	63621-356-25	openfda.package_ndc
ndc	package	63621-356-30	openfda.package_ndc
ndc	product	63621-356	openfda.product_ndc
ndc11	package	63621035630	derived:openfda.package_ndc
ndc11	package	63621035650	derived:openfda.package_ndc
ndc11	package	63621035620	derived:openfda.package_ndc
ndc11	package	63621035625	derived:openfda.package_ndc
ndc11	package	63621035614	derived:openfda.package_ndc
ndc11	package	63621035640	derived:openfda.package_ndc
rxcui		581658	openfda.rxcui
spl id		435330fc-c021-151b-e063-6394a90a229b	id
spl set id		b0623424-939e-4b49-aa99-c1ef22cf0f2d	set_id
unii		3K9958V90M	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 Flammable. Keep away from fire or flame. For external use only. If swallowed, seek medical attention. When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact doctor immediately. Stop use and consult a doctor when skin irritation appears and lasts. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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