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
- NuCare Pharmaceuticals,Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f9b4d18b-25f3-604f-e053-6394a90a5531
- SPL ID
- 2dcdd631-b9c5-e301-e063-6294a90a038f
- Version
- 2
- Effective date
- 2025-02-10
- 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 06:16:07
| 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 | NuCare Pharmaceuticals,Inc. | openfda.manufacturer_name | |
| ndc | package | 68071-2984-5 | openfda.package_ndc |
| ndc | product | 68071-2984 | openfda.product_ndc |
| ndc11 | package | 68071298405 | derived:openfda.package_ndc |
| rxcui | 197305 | openfda.rxcui | |
| spl id | 2dcdd631-b9c5-e301-e063-6294a90a038f | id | |
| spl set id | f9b4d18b-25f3-604f-e053-6394a90a5531 | 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.