Steritalc 2g
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Steritalc 2g
- Generic name
- TALC
- Manufacturer
- Novatech SA
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c94e51d9-beef-4b06-e053-2a95a90a754a
- SPL ID
- 386130d4-1b0d-5e87-e063-6394a90aefa7
- Version
- 7
- Effective date
- 2025-06-25
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:19:03
| Harmonized routes |
|---|
| INTRAPLEURAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | NDA | 205555 | derived:openfda.application_number |
| application number | NDA205555 | openfda.application_number | |
| brand name | Steritalc 3g | openfda.brand_name | |
| brand name | Steritalc 2g | openfda.brand_name | |
| brand name | Steritalc 4g | openfda.brand_name | |
| generic name | TALC | openfda.generic_name | |
| manufacturer name | Novatech SA | openfda.manufacturer_name | |
| ndc | package | 62327-333-03 | openfda.package_ndc |
| ndc | package | 62327-444-04 | openfda.package_ndc |
| ndc | package | 62327-222-02 | openfda.package_ndc |
| ndc | package | 62327-444-44 | openfda.package_ndc |
| ndc | package | 62327-333-43 | openfda.package_ndc |
| ndc | package | 62327-222-42 | openfda.package_ndc |
| ndc | product | 62327-333 | openfda.product_ndc |
| ndc | product | 62327-222 | openfda.product_ndc |
| ndc | product | 62327-444 | openfda.product_ndc |
| ndc11 | package | 62327033303 | derived:openfda.package_ndc |
| ndc11 | package | 62327033343 | derived:openfda.package_ndc |
| ndc11 | package | 62327022242 | derived:openfda.package_ndc |
| ndc11 | package | 62327044404 | derived:openfda.package_ndc |
| ndc11 | package | 62327022202 | derived:openfda.package_ndc |
| ndc11 | package | 62327044444 | derived:openfda.package_ndc |
| rxcui | 2003393 | openfda.rxcui | |
| rxcui | 2003405 | openfda.rxcui | |
| rxcui | 2003402 | openfda.rxcui | |
| rxcui | 2003403 | openfda.rxcui | |
| rxcui | 2003400 | openfda.rxcui | |
| rxcui | 2003398 | openfda.rxcui | |
| spl id | 386130d4-1b0d-5e87-e063-6394a90aefa7 | id | |
| spl set id | c94e51d9-beef-4b06-e053-2a95a90a754a | set_id | |
| unii | 7SEV7J4R1U | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5. WARNINGS AND PRECAUTIONS 5.1 Pneumonitis and Acute Respiratory Distress Syndrome (ARDS) Acute Pneumonitis and ARDS, including fatal cases, have been reported with intrapleural use of various talc products. Systemic exposure of talc could be affected by the integrity of the visceral pleura and could be increased if talc is administered immediately after mechanical abrasion or biopsy of the pleura. The literature also suggests a possible correlation between talc particle size distribution and risk of toxicity. There are published reports of two large, prospective trials conducted to evaluate the safety of STERITALC administered intrapleurally. One trial evaluated 558 patients treated with STERITALC 4g by poudrage for MPE. The second trial evaluated 418 patients with recurrent primary spontaneous pneumothorax treated with STERITALC 2 g by poudrage. No cases of ARDS or talc-related lung injury were reported. 5.2 Interference with Future Procedures Sclerosis of the pleural space may preclude or complicate subsequent ipsilateral surgery and diagnostic procedures. Consider the possible effects of the use of STERITALC on future diagnostic and therapeutic procedures prior to administration. 5.3 Lead Content Lead is present in STERITALC as an impurity. The main target organ for lead toxicity is the nervous system, but effects of lead exposure also include increased blood pressure, anemia, decreased sperm production, and damage to the kidneys in children and adults. Minimal risk levels of lead have not been derived for humans because clear thresholds for effects have not been identified. Children are more sensitive to lead toxicity than adults, and no safe blood level has been determined in children. Cognitive and neurobehavioral deficits are observed in children exposed to lead. Exposure of a pregnant woman to lead may cause miscarriage, premature birth, lower birth weights and slow or impaired mental development in the child. Administration of STERITALC at the highest recommended dose of 10 grams may deliver up to 40 mcg of lead. 5.4 Asbestos Content Talc products may contain trace amounts of asbestos. Asbestos is a known human carcinogen. Exposure to asbestos may increase the risk of mesotheliomas and other cancers including lung, larynx, and ovarian cancer. STERITALC is tested for asbestos and asbestiform fibers [see DESCRIPTION (11)]. _ ______WARNINGS AND PRECAUTIONS _____________ Pneumonitis and Acute Respiratory Distress Syndrome (ARDS): Acute Pneumonitis and ARDS, have been reported with intrapleural use of various talc products. (5.1) Interference with Future Procedures: Sclerosis of the pleural space may preclude or complicate subsequent ipsilateral surgery and diagnostic procedures. (5.2) Lead Content: STERITALC® contains lead as an impurity. May cause lead toxicity, especially in children. (5.3) Asbestos Content: Talc products may contain trace amounts of asbestos. Exposure to asbestos may increase the risk of mesotheliomas and other cancers. (5.4, 11)
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6. ADVERSE REACTIONS The following clinically significant adverse reactions are described elsewhere in the labeling. Pneumonitis and Acute Respiratory Distress Syndrome (ARDS) [see Warnings and Precautions (5.1)] Lead Content [see Warnings and Precautions (5.3)] Asbestos Content [see Warnings and Precautions (5.4)] Common adverse reactions observed with intrapleural use of various talc products are fever and pain. Other adverse reactions include dyspnea, arrhythmia, empyema, pneumonitis and acute respiratory distress syndrome (ARDS). Procedure related adverse reactions such as bleeding, hemothorax, wound infections, atelectasis and pneumonia may occur. _____________ ADVERSE REACTIONS _____________ Common adverse reactions are fever and pain. (6) To report suspected adverse reactions contact Boston Medical Product Inc., at 508-898-9300 and FDA at 1-800-332-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.