warnings
Warnings For external use only
Aquaphor Itch Relief
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
- Aquaphor Itch Relief
- Generic name
- HYDROCORTISONE
- Manufacturer
- Beiersdorf Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b1d0333f-ba60-35d8-e053-2995a90af932
- SPL ID
- 4615f353-0a2d-5ff1-e063-6394a90a77e3
- Version
- 6
- Effective date
- 2025-12-16
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:46:34
| 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 | M017 | openfda.application_number | |
| brand name | Aquaphor Itch Relief | openfda.brand_name | |
| generic name | HYDROCORTISONE | openfda.generic_name | |
| manufacturer name | Beiersdorf Inc | openfda.manufacturer_name | |
| ndc | package | 10356-120-52 | openfda.package_ndc |
| ndc | package | 10356-120-30 | openfda.package_ndc |
| ndc | package | 10356-120-07 | openfda.package_ndc |
| ndc | package | 10356-120-53 | openfda.package_ndc |
| ndc | package | 10356-120-04 | openfda.package_ndc |
| ndc | package | 10356-120-54 | openfda.package_ndc |
| ndc | product | 10356-120 | openfda.product_ndc |
| ndc11 | package | 10356012030 | derived:openfda.package_ndc |
| ndc11 | package | 10356012052 | derived:openfda.package_ndc |
| ndc11 | package | 10356012054 | derived:openfda.package_ndc |
| ndc11 | package | 10356012053 | derived:openfda.package_ndc |
| ndc11 | package | 10356012007 | derived:openfda.package_ndc |
| ndc11 | package | 10356012004 | derived:openfda.package_ndc |
| rxcui | 2462510 | openfda.rxcui | |
| rxcui | 203105 | openfda.rxcui | |
| spl id | 4615f353-0a2d-5ff1-e063-6394a90a77e3 | id | |
| spl set id | b1d0333f-ba60-35d8-e053-2995a90af932 | set_id | |
| unii | WI4X0X7BPJ | 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.