Quality Choice Instant Ear Dry
Quality Choice Instant Ear Dry is an FDA drug label for the active ingredient ISOPROPYL ALCOHOL manufactured by Chain Drug Manufacturing Association administered by AURICULAR (OTIC). 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 20231220.
- Generic name
- ISOPROPYL ALCOHOL
- Manufacturer
- Chain Drug Manufacturing Association
- Product type
- HUMAN OTC DRUG
- Route
- AURICULAR (OTIC)
- Dosage form
- N/A
- NDC
- 63868-408
- Application
- M014
- Label effective
- 20231220
About this product
Quality Choice Instant Ear Dry is an FDA-registered drug product whose active ingredient is ISOPROPYL ALCOHOL. It is labelled by Chain Drug Manufacturing Association taken by auricular (otic) and marketed as a human otc drug product. Identifiers on file: NDC 63868-408, application M014, label effective 20231220. 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: dries water. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use Dries water in the ears.
Dosage & Administration
Directions Apply 5 to 5 drops in each affected ear..
Warnings
Warnings Flammable : Keep away from fire and flame. Do not use in the eyes. Ask a doctor before use if you have Ear drainage or discharge. Pain, irritation, or rash in the ear. Have had ear surgery. Dizziness. Stop use and ask doctor if Irritation (too much burning) or pain occurs. Keep out of reach of children. In case of accidental ingestion, seek professional assistant or contact a Poison Control Center immediately.
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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 Quality Choice Instant Ear Dry used for?
Use Dries water in the ears.
Who makes Quality Choice Instant Ear Dry?
Chain Drug Manufacturing Association is the labeler of record for Quality Choice Instant Ear Dry. 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 Quality Choice Instant Ear Dry come in?
administered by auricular (otic). Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Quality Choice Instant Ear Dry 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 Quality Choice Instant Ear Dry 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.