warnings
Warnings: Keep out of reach of children. Ingestion will result in a severe gastrointestinal distress, unconsciousness and death. If ingested induce vomiting if victim is conscious. Contact a poison control center immediately.
Compound Benzoin Tincture
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
- Compound Benzoin Tincture
- Generic name
- TINCTURE OF BENZOIN
- Manufacturer
- Medical Chemical Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 243494ee-342d-4c32-9a86-f8c6c347bd8b
- SPL ID
- 55933c46-b6ef-7902-e063-6394a90a61c7
- Version
- 19
- Effective date
- 2026-07-01
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:17
| Harmonized routes |
|---|
| TOPICAL |
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 number | M003 | openfda.application_number | |
| brand name | Compound Benzoin Tincture | openfda.brand_name | |
| generic name | TINCTURE OF BENZOIN | openfda.generic_name | |
| manufacturer name | Medical Chemical Corporation | openfda.manufacturer_name | |
| ndc | package | 12745-109-04 | openfda.package_ndc |
| ndc | package | 12745-109-02 | openfda.package_ndc |
| ndc | package | 12745-109-01 | openfda.package_ndc |
| ndc | package | 12745-109-03 | openfda.package_ndc |
| ndc | product | 12745-109 | openfda.product_ndc |
| ndc11 | package | 12745010904 | derived:openfda.package_ndc |
| ndc11 | package | 12745010903 | derived:openfda.package_ndc |
| ndc11 | package | 12745010902 | derived:openfda.package_ndc |
| ndc11 | package | 12745010901 | derived:openfda.package_ndc |
| rxcui | 562404 | openfda.rxcui | |
| spl id | 55933c46-b6ef-7902-e063-6394a90a61c7 | id | |
| spl set id | 243494ee-342d-4c32-9a86-f8c6c347bd8b | set_id | |
| unii | GK21SBA74R | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.