Spot Correction
Spot Correction is an FDA drug label for the active ingredient SULFUR manufactured by HydroPeptide LLC 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 20260812.
- Generic name
- SULFUR
- Manufacturer
- HydroPeptide LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 60934-002
- Application
- M006
- Label effective
- 20260812
About this product
Spot Correction is an FDA-registered drug product whose active ingredient is SULFUR. It is labelled by HydroPeptide LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 60934-002, application M006, label effective 20260812. It is one of 37 FDA drug label records sharing the active ingredient SULFUR. 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 SULFUR are most often described in connection with: treats acne, helps prevent, new pimples. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses treats acne helps prevent new pimples clears up most acne pimples
Dosage & Administration
Directions clean the skin thoroughly before applying this product cover the entire affected area with a thin layer one to three times daily. because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor if bothersome dryness or peeling occurs, reduce application to once a day or every other day
Warnings
Warnings For external use only Do not use on: broken skin large areas of the body When applying this product apply only to areas with acne rinse right away with water if it gets in eyes skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. Stop use and ask a doctor if skin irritation occurs or gets worse Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
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View labelAcne Treatment with Sulfur
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View labelGlovers Dandruff Control Med., Floral
View labelGlovers Dandruff Control Medicine, Regular
View labelHow products containing SULFUR compare
FDA lists 37 drug label records with SULFUR 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 |
|---|---|---|---|
| — | — | Boiron | 12 |
| — | — | Nature's Innovation, Inc. | 5 |
| — | — | J. Strickland & Co. | 4 |
| — | — | L'Oreal USA Products Inc | 2 |
| — | — | 111MedCo LLC | 1 |
Frequently asked questions
What is Spot Correction used for?
Uses treats acne helps prevent new pimples clears up most acne pimples
Who makes Spot Correction?
HydroPeptide LLC is the labeler of record for Spot Correction. 37 FDA label records share the active ingredient SULFUR, 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 Spot Correction 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 Spot Correction 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 SULFUR?
Yes. 37 FDA drug label records list SULFUR 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 Spot Correction 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.