91% 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
91% Isopropyl Alcohol
Generic name
ISOPROPYL ALCOHOL
Manufacturer
Chain Drug Marketing Association
Product type
HUMAN OTC DRUG
SPL set ID
f10995fd-fe94-436a-8783-4cdf10438d75
SPL ID
51c8b124-75cc-384c-e063-6294a90ad4de
Version
4
Effective date
2026-05-14
Source export date
2026-10-30
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/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:36:48
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 do not use as fuel source. If exposed to a heat source, vapors may ignite, resulting in severe burns, serious injury, or death.

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#

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

adverse reactions

Adverse reaction QC 100% Satisfaction Guaranteed Distributed by CDMA, Inc. Novi, MI 48375 www.qualitychoice.com Questions: 800-935-2382 Pat. D675,101

Reported adverse events (FAERS/openFDA)#

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