warnings
Warnings For external use only.
Quality Choice Iodides 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
- Quality Choice Iodides Tincture
- Generic name
- ETHYL ALCOHOL
- Manufacturer
- Chain Drug Market Association
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 71aedfd5-e81f-4b69-b163-527ff1ce30b1
- SPL ID
- 0cf4bfe6-384f-e836-e063-6394a90ab8c3
- Version
- 6
- Effective date
- 2023-12-20
- Source export date
- 2026-10-27
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/a73bb3b6a943796a18cd4bcd0917240b579be4636d00e6e39481bafbd8093f69/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:33:37
| 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 | Quality Choice Iodides Tincture | openfda.brand_name | |
| generic name | ETHYL ALCOHOL | openfda.generic_name | |
| manufacturer name | Chain Drug Market Association | openfda.manufacturer_name | |
| ndc | package | 63868-331-02 | openfda.package_ndc |
| ndc | product | 63868-331 | openfda.product_ndc |
| ndc11 | package | 63868033102 | derived:openfda.package_ndc |
| spl id | 0cf4bfe6-384f-e836-e063-6394a90ab8c3 | id | |
| spl set id | 71aedfd5-e81f-4b69-b163-527ff1ce30b1 | set_id | |
| unii | 3K9958V90M | 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.