warnings
For external use only
MG217 Eczema Face
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
- MG217 Eczema Face
- Generic name
- COLLOIDAL OATMEAL
- Manufacturer
- Wisconsin Pharmacal Company
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5f10697e-7f0c-f2b7-e053-2991aa0aabde
- SPL ID
- 5f3c3d06-3e3f-1f9d-e053-2991aa0a02d1
- Version
- 4
- Effective date
- 2017-11-30
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:31:57
| 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 | part347 | openfda.application_number | |
| brand name | MG217 Eczema Face | openfda.brand_name | |
| generic name | COLLOIDAL OATMEAL | openfda.generic_name | |
| manufacturer name | Wisconsin Pharmacal Company | openfda.manufacturer_name | |
| ndc | package | 68093-7245-1 | openfda.package_ndc |
| ndc | product | 68093-7245 | openfda.product_ndc |
| ndc11 | package | 68093724501 | derived:openfda.package_ndc |
| rxcui | 1591951 | openfda.rxcui | |
| spl id | 5f3c3d06-3e3f-1f9d-e053-2991aa0a02d1 | id | |
| spl set id | 5f10697e-7f0c-f2b7-e053-2991aa0aabde | set_id | |
| unii | 8PI54V663Y | 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.