STASIS
STASIS is an FDA drug label for the active ingredient FERRIC SULFATE manufactured by Gingi-Pak a Division of the Belport administered by DENTAL. 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 20260501.
- Generic name
- FERRIC SULFATE
- Manufacturer
- Gingi-Pak a Division of the Belport
- Product type
- HUMAN OTC DRUG
- Route
- DENTAL
- Dosage form
- N/A
- NDC
- 10129-031
- Application
- N/A
- Label effective
- 20260501
About this product
STASIS is an FDA-registered drug product whose active ingredient is FERRIC SULFATE. It is labelled by Gingi-Pak a Division of the Belport taken by dental and marketed as a human otc drug product. Identifiers on file: NDC 10129-031, label effective 20260501. 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.
Active ingredients
Indications & Usage
Uses Uses
Dosage & Administration
Directions Directions
Warnings
Warning Warnings
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-0416-2021 | RESTASIS 0.05%30X 0.4ML OPTH PF; NDC/UPC 23916330; RX; DROPS/Restasis 0.05% 60x0.4 mL OPTH PF; NDC/UPC 23916330; RX | Cardinal Health Inc. | Class II | Terminated | 20210602 |
Frequently asked questions
What is STASIS used for?
Uses Uses
Who makes STASIS?
Gingi-Pak a Division of the Belport is the labeler of record for STASIS.
What form does STASIS come in?
administered by dental. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is STASIS 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.
Has STASIS 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.