warnings
Warnings For external use only
Family Care Anti-Itch
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
- Family Care Anti-Itch
- Generic name
- HYDROCORTISONE
- Manufacturer
- United Exchange Corp.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- deb09e89-9794-89a7-e053-2a95a90abdf8
- SPL ID
- 41a0205a-ccd4-7837-e063-6294a90a9746
- Version
- 3
- Effective date
- 2025-10-20
- 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 06:16:46
| 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 | Family Care Anti-Itch | openfda.brand_name | |
| generic name | HYDROCORTISONE | openfda.generic_name | |
| manufacturer name | United Exchange Corp. | openfda.manufacturer_name | |
| ndc | package | 65923-494-14 | openfda.package_ndc |
| ndc | product | 65923-494 | openfda.product_ndc |
| ndc11 | package | 65923049414 | derived:openfda.package_ndc |
| rxcui | 106258 | openfda.rxcui | |
| spl id | 41a0205a-ccd4-7837-e063-6294a90a9746 | id | |
| spl set id | deb09e89-9794-89a7-e053-2a95a90abdf8 | 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.