warnings
Warnings For external use only.
Micro-Guard (AF)
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
- Micro-Guard (AF)
- Generic name
- MICONAZOLE NITRATE
- Manufacturer
- Coloplast Corp
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a43a94d0-fec0-470f-bdb4-535dcce6d1e0
- SPL ID
- ecd660df-c2f6-4a4c-b878-4451869d9770
- Version
- 8
- Effective date
- 2026-03-27
- 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 06:18:58
| 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 | M005 | openfda.application_number | |
| brand name | Micro-Guard (AF) | openfda.brand_name | |
| generic name | MICONAZOLE NITRATE | openfda.generic_name | |
| manufacturer name | Coloplast Corp | openfda.manufacturer_name | |
| ndc | package | 11701-038-16 | openfda.package_ndc |
| ndc | product | 11701-038 | openfda.product_ndc |
| ndc11 | package | 11701003816 | derived:openfda.package_ndc |
| rxcui | 998469 | openfda.rxcui | |
| rxcui | 998461 | openfda.rxcui | |
| spl id | ecd660df-c2f6-4a4c-b878-4451869d9770 | id | |
| spl set id | a43a94d0-fec0-470f-bdb4-535dcce6d1e0 | set_id | |
| unii | VW4H1CYW1K | 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.