Midnight Magic Hand Sanitizer
Midnight Magic Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by Scent Theory Products 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 20260721.
- Generic name
- ALCOHOL
- Manufacturer
- Scent Theory Products LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 76891-182
- Application
- M003
- Label effective
- 20260721
About this product
Midnight Magic Hand Sanitizer is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Scent Theory Products LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 76891-182, application M003, label effective 20260721. It is one of 582 FDA drug label records sharing the active ingredient 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 ALCOHOL are most often described in connection with: handwashing decrease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For handwashing to decrease bacteria on the skin.
Dosage & Administration
Directions Spray hands with product and allow to dry without wiping For children under 6, use only under adult supervision Not recommended for infants
Warnings
Warnings For external use only: hands Flammable, keep away from fire or flame. When using this product - keep out of eyes. In case of contact with eyes, flush thoroughly with water. - avoid contact with broken skin. - do not inhale or ingest. Stop use and ask a doctor if - irritation and redness develop - condition persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.
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View labelHow products containing ALCOHOL compare
FDA lists 582 drug label records with 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 |
|---|---|---|---|
| — | — | Bath & Body Works, Inc. | 79 |
| — | — | Shenzhen Lantern Scicence Co.,Ltd. | 66 |
| — | — | Fourstar Group USA, Inc. | 41 |
| — | — | Church & Dwight Co., Inc. | 33 |
| — | — | Target Corporation | 23 |
Frequently asked questions
What is Midnight Magic Hand Sanitizer used for?
Uses For handwashing to decrease bacteria on the skin.
Who makes Midnight Magic Hand Sanitizer?
Scent Theory Products LLC is the labeler of record for Midnight Magic Hand Sanitizer. 582 FDA label records share the active ingredient 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 Midnight Magic Hand Sanitizer 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 Midnight Magic Hand Sanitizer 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 ALCOHOL?
Yes. 582 FDA drug label records list 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 Midnight Magic Hand Sanitizer 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.