warnings
Warnings For External Use Only Do not use In the genital area if you have a vaginal discharge.
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
- Itch Relief
- Generic name
- HYDROCORTISONE 1%
- Manufacturer
- Trifecta Pharmaceuticals USA LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- af5daf6c-bcad-8ebf-e053-2a95a90af1b0
- SPL ID
- 29b36988-b625-40f2-e063-6294a90a39b8
- Version
- 3
- Effective date
- 2024-12-20
- Source export date
- 2026-10-30
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/eb45a4bb6908a5d117668eac8da5ce490c753c3f9b68298758ef131307d1d264/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:17:37
| 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 | Itch Relief | openfda.brand_name | |
| generic name | HYDROCORTISONE 1% | openfda.generic_name | |
| manufacturer name | Trifecta Pharmaceuticals USA LLC | openfda.manufacturer_name | |
| ndc | package | 69396-057-01 | openfda.package_ndc |
| ndc | product | 69396-057 | openfda.product_ndc |
| ndc11 | package | 69396005701 | derived:openfda.package_ndc |
| rxcui | 106258 | openfda.rxcui | |
| spl id | 29b36988-b625-40f2-e063-6294a90a39b8 | id | |
| spl set id | af5daf6c-bcad-8ebf-e053-2a95a90af1b0 | 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.