Isopropyl Alcohol

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
Isopropyl Alcohol
Generic name
ISOPROPYL ALCOHOL
Manufacturer
Dyad Medical Sourcing, LLC
Product type
HUMAN OTC DRUG
SPL set ID
b5c9e222-10eb-4cea-af70-213a77fcc865
SPL ID
4a0310ad-f209-9469-e063-6294a90a3282
Version
13
Effective date
2026-02-04
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:30:26
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 · 2 matching rows.

warnings

Warnings For external use only. If taken internally serious gastric disturbances will result. Flammable Keep away from fire or flame, heat, spark, electrical

warnings and cautions

Caution Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Adverse reactions cross-check#

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

ADVERSE REACTION Manufactured for: Dyad Medical Sourcing, LLC 2101 Waukegan Road, Suite 208, Bannokburn, IL 60015 1-855-241-1773, info@dyadms.com Made in the USA with US and foreign components #901-HCS0203 Rev. 0 2018 Dyad Medical Sourcing, LLC Pat. D675, 101

Reported adverse events (FAERS/openFDA)#

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