QVE - S

SODIUM CHLORITE TOPICAL HUMAN OTC DRUG

QVE - S is an FDA drug label for the active ingredient SODIUM CHLORITE manufactured by Pure O2 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 20200814.

Generic name
SODIUM CHLORITE
Manufacturer
Pure O2
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
75124-0010
Application
N/A
Label effective
20200814

About this product

QVE - S is an FDA-registered drug product whose active ingredient is SODIUM CHLORITE. It is labelled by Pure O2 taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 75124-0010, label effective 20200814. It is one of 11 FDA drug label records sharing the active ingredient SODIUM CHLORITE. 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 SODIUM CHLORITE are most often described in connection with: please see, label attached. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

sodium chlorite

Indications & Usage

please see the label attached

Dosage & Administration

for external use only

Warnings

■ For external use only. ■ Do not use in eyes. ■ lf swallowed, get medical help promptly. ■ Stop use, ask doctor lf irritation occurs. ■ Keep out of reach of children.

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How products containing SODIUM CHLORITE compare

FDA lists 11 drug label records with SODIUM CHLORITE 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 formProductsManufacturerProducts
— — Pure O2 11
— — — —
— — — —
— — — —
— — — —

Frequently asked questions

What is QVE - S used for?
please see the label attached

Who makes QVE - S?
Pure O2 is the labeler of record for QVE - S. 11 FDA label records share the active ingredient SODIUM CHLORITE, 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 QVE - S 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 QVE - S 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 SODIUM CHLORITE?
Yes. 11 FDA drug label records list SODIUM CHLORITE 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 QVE - S 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.