warnings
Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.
D-83-1
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
- D-83-1
- Generic name
- CANDIDA ALBICANS
- Manufacturer
- DNA Labs, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 6f922b3c-cd6b-48c9-9bf9-0da8f061ac1e
- SPL ID
- 2b9ec8dd-73b3-e366-e063-6394a90ae792
- Version
- 3
- Effective date
- 2025-01-13
- 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 05:18:15
| Harmonized routes |
|---|
| SUBLINGUAL |
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 |
|---|---|---|---|
| brand name | D-83-1 | openfda.brand_name | |
| generic name | CANDIDA ALBICANS | openfda.generic_name | |
| manufacturer name | DNA Labs, Inc. | openfda.manufacturer_name | |
| ndc | package | 58264-0085-1 | openfda.package_ndc |
| ndc | product | 58264-0085 | openfda.product_ndc |
| ndc11 | package | 58264008501 | derived:openfda.package_ndc |
| spl id | 2b9ec8dd-73b3-e366-e063-6394a90ae792 | id | |
| spl set id | 6f922b3c-cd6b-48c9-9bf9-0da8f061ac1e | set_id | |
| unii | 4D7G21HDBC | 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.