warnings
WARNINGS Discontinue promptly if sensitization or irritation occurs.
Acetic Acid
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
- Acetic Acid
- Generic name
- ACETIC ACID
- Manufacturer
- A-S Medication Solutions
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c1c28375-9b03-4590-9d39-ab28403da93d
- SPL ID
- 9e3367b4-c357-4ecf-90da-5fd1da2bc2b7
- Version
- 3
- Effective date
- 2026-03-18
- 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 05:20:16
| Harmonized routes |
|---|
| AURICULAR (OTIC) |
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 | 040607 | derived:openfda.application_number |
| application number | ANDA040607 | openfda.application_number | |
| brand name | Acetic Acid | openfda.brand_name | |
| generic name | ACETIC ACID | openfda.generic_name | |
| manufacturer name | A-S Medication Solutions | openfda.manufacturer_name | |
| ndc | package | 50090-6527-0 | openfda.package_ndc |
| ndc | product | 50090-6527 | openfda.product_ndc |
| ndc11 | package | 50090652700 | derived:openfda.package_ndc |
| rxcui | 197305 | openfda.rxcui | |
| spl id | 9e3367b4-c357-4ecf-90da-5fd1da2bc2b7 | id | |
| spl set id | c1c28375-9b03-4590-9d39-ab28403da93d | set_id | |
| unii | Q40Q9N063P | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Stinging or burning may be noted occasionally; local irritation has occurred very rarely. To report SUSPECTED ADVERSE REACTIONS, contact Saptalis Pharmaceuticals, LLC at 1-833-727-8254 or FDA at 1800-FDA-1088 or www.fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.