DOP Ethyl Alcohol 70%

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
DOP Ethyl Alcohol 70%
Generic name
ETHYL ALCOHOL
Manufacturer
Omega & Delta Co., Inc.
Product type
HUMAN OTC DRUG
SPL set ID
b96d85f8-739c-4b96-9dd5-8119ebf66c9f
SPL ID
28caf8eb-1b93-4d28-b12d-22c5eda9bf8a
Version
1
Effective date
2026-01-21
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:18:58
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 For external use only Flammable keep away from fire or flame, heat, spark, electrical Ask a doctor before use for deep wounds, animal bites or serious burns When using this product • do not get into eyes • do not apply over large area of the body • do not use longer than 1 week Stop use and ask a doctor if the condition persists or gets worse

Reported adverse events (FAERS/openFDA)#

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