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
2026-08-01
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/2026-08-01/5a565ce64c898c83223b815b9579cd46fb0c6d54977c3cace2133e40124f7fbb/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:10:32
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 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.