lumicain
lumicain is an FDA drug label for the active ingredient ALUMINIUM CHLORIDE HEXAHYDRATE manufactured by Medical Products Laboratories, Inc. 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 20201223.
- Generic name
- ALUMINIUM CHLORIDE HEXAHYDRATE
- Manufacturer
- Medical Products Laboratories, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 10733-412
- Application
- N/A
- Label effective
- 20201223
About this product
lumicain is an FDA-registered drug product whose active ingredient is ALUMINIUM CHLORIDE HEXAHYDRATE. It is labelled by Medical Products Laboratories, Inc. taken by topical and marketed as a human prescription drug product. Identifiers on file: NDC 10733-412, label effective 20201223. 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.
Dosage & Administration
FOR TOPICAL APPLICATION ONLY For Granulation Tissue Growth: Allow packing saturated in Lumicain to remain in nail groove for 48 hours; repeat if necessary. If hemmorrhage is profuse, dress wound with gauze saturated with Lumicain and allow to remain for 24 hours or longer.
Recall and safety notices
1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0179-2026 | Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01 | Medical Products Laboratories, Inc. | Class II | Ongoing | 20251203 |
Frequently asked questions
What is lumicain used for?
No indications section is present in the FDA label on file for this product. Consult the prescribing information supplied with the medicine or ask a pharmacist.
Who makes lumicain?
Medical Products Laboratories, Inc. is the labeler of record for lumicain.
What form does lumicain 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 lumicain prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has lumicain been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
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.