warnings
Warnings For external use only
Eczema Relief Cream Body Wash
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
- Eczema Relief Cream Body Wash
- Generic name
- OATMEAL
- Manufacturer
- Beiersdorf Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f12644e5-0ff0-de0e-e053-2995a90a0995
- SPL ID
- 474aa265-c89d-6c11-e063-6294a90a6f4f
- Version
- 5
- Effective date
- 2025-12-31
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:34:55
| 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 | M016 | openfda.application_number | |
| brand name | Eczema Relief Cream Body Wash | openfda.brand_name | |
| generic name | OATMEAL | openfda.generic_name | |
| manufacturer name | Beiersdorf Inc | openfda.manufacturer_name | |
| ndc | package | 10356-382-26 | openfda.package_ndc |
| ndc | product | 10356-382 | openfda.product_ndc |
| ndc11 | package | 10356038226 | derived:openfda.package_ndc |
| rxcui | 2172890 | openfda.rxcui | |
| spl id | 474aa265-c89d-6c11-e063-6294a90a6f4f | id | |
| spl set id | f12644e5-0ff0-de0e-e053-2995a90a0995 | 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.