91% Isopropyl Alcohol
91% Isopropyl Alcohol is an FDA drug label for the active ingredient ISOPROPYL ALCOHOL manufactured by Chain Drug Marketing Association administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260514.
- Generic name
- ISOPROPYL ALCOHOL
- Manufacturer
- Chain Drug Marketing Association
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 83324-173
- Application
- M003
- Label effective
- 20260514
About this product
91% Isopropyl Alcohol is an FDA-registered drug product whose active ingredient is ISOPROPYL ALCOHOL. It is labelled by Chain Drug Marketing Association taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83324-173, application M003, label effective 20260514. It is one of 128 FDA drug label records sharing the active ingredient ISOPROPYL ALCOHOL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ISOPROPYL ALCOHOL are most often described in connection with: first aid, help prevent, risk infection, minor cuts, scrapes burns. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns
Dosage & Administration
Directions clean the affected area apply a small amount of this product on the affected area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first
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.
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
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View labelHow products containing ISOPROPYL ALCOHOL compare
FDA lists 128 drug label records with ISOPROPYL ALCOHOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Jianerkang Medical Co., Ltd | 14 |
| — | — | Medline Industries, LP | 4 |
| — | — | Pharma Nobis, LLC | 4 |
| — | — | Strategic Sourcing Services LLC | 4 |
| — | — | ADUSA Distribution, LLC | 3 |
Frequently asked questions
What is 91% Isopropyl Alcohol used for?
Uses first aid to help prevent the risk of infection in: minor cuts scrapes burns
Who makes 91% Isopropyl Alcohol?
Chain Drug Marketing Association is the labeler of record for 91% Isopropyl Alcohol. 128 FDA label records share the active ingredient ISOPROPYL ALCOHOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does 91% Isopropyl Alcohol come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is 91% Isopropyl Alcohol prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing ISOPROPYL ALCOHOL?
Yes. 128 FDA drug label records list ISOPROPYL ALCOHOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has 91% Isopropyl Alcohol been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.