Acetylcysteine
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
- Acetylcysteine
- Generic name
- ACETYLCYSTEINE
- Manufacturer
- Somerset Therapeutics, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d50c8ab6-26f8-4669-89d1-c4d26698159a
- SPL ID
- af1a403e-02e4-4d18-bb00-6629a8e7c261
- Version
- 7
- Effective date
- 2026-04-11
- Source export date
- 2026-09-28
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:19:14
| Harmonized routes |
|---|
| RESPIRATORY (INHALATION) |
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 | ANDA | 219194 | derived:openfda.application_number |
| application number | ANDA219194 | openfda.application_number | |
| brand name | Acetylcysteine | openfda.brand_name | |
| generic name | ACETYLCYSTEINE | openfda.generic_name | |
| manufacturer name | Somerset Therapeutics, LLC | openfda.manufacturer_name | |
| ndc | package | 70069-018-25 | openfda.package_ndc |
| ndc | package | 70069-020-03 | openfda.package_ndc |
| ndc | package | 70069-020-01 | openfda.package_ndc |
| ndc | package | 70069-018-01 | openfda.package_ndc |
| ndc | package | 70069-019-01 | openfda.package_ndc |
| ndc | package | 70069-019-25 | openfda.package_ndc |
| ndc | product | 70069-019 | openfda.product_ndc |
| ndc | product | 70069-020 | openfda.product_ndc |
| ndc | product | 70069-018 | openfda.product_ndc |
| ndc11 | package | 70069001925 | derived:openfda.package_ndc |
| ndc11 | package | 70069001801 | derived:openfda.package_ndc |
| ndc11 | package | 70069001901 | derived:openfda.package_ndc |
| ndc11 | package | 70069001825 | derived:openfda.package_ndc |
| ndc11 | package | 70069002003 | derived:openfda.package_ndc |
| ndc11 | package | 70069002001 | derived:openfda.package_ndc |
| rxcui | 307718 | openfda.rxcui | |
| rxcui | 307719 | openfda.rxcui | |
| spl id | af1a403e-02e4-4d18-bb00-6629a8e7c261 | id | |
| spl set id | d50c8ab6-26f8-4669-89d1-c4d26698159a | set_id | |
| unii | WYQ7N0BPYC | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS After proper administration of acetylcysteine solution, an increased volume of liquified bronchial secretions may occur. When cough is inadequate, the airway must be maintained open by mechanical suction if necessary. Where there is a mechanical block due to foreign body or local accumulation, the airway should be cleared by endotracheal aspiration, with or without bronchoscopy. Asthmatics under treatment with acetylcysteine solution should be watched carefully. Most patients with bronchospasm are quickly relieved by the use of a bronchodilator given by nebulization. If bronchospasm progresses, the medication should be discontinued immediately.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Adverse effects have included stomatitis, nausea, vomiting, fever, rhinorrhea, drowsiness, clamminess, chest tightness, and bronchoconstriction. Clinically overt acetylcysteine solution induced bronchospasm occurs infrequently and unpredictably even in patients with asthmatic bronchitis or bronchitis complicating bronchial asthma. Acquired sensitization to acetylcysteine solution has been reported rarely. Reports of sensitization in patients have not been confirmed by patch testing. Sensitization has been confirmed in several inhalation therapists who reported a history of dermal eruptions after frequent and extended exposure to acetylcysteine solution. Reports of irritation to the tracheal and bronchial tracts have been received and although hemoptysis has occurred in patients receiving acetylcysteine solution such findings are not uncommon in patients with bronchopulmonary disease and a causal relationship has not been established. To report SUSPECTED ADVERSE REACTIONS, contact Somerset Therapeutics, LLC at 1- 800-417-9175 or FDA at 1-800 -FDA-1088 or www.fda.gov/medwatch
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.