warnings
Warnings:
Diphenhydramine HCL
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
- Diphenhydramine HCL
- Generic name
- DIPHENHYDRAMINE HCL
- Manufacturer
- NuCare Pharmaceuticals, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3dbdf020-ca17-1197-e054-00144ff8d46c
- SPL ID
- 1f98d6d5-cf09-a2bf-e063-6294a90a370b
- Version
- 4
- Effective date
- 2024-08-13
- Source export date
- 2026-10-27
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/2c7d3f7bcea1543046130e07dcbaf7eea5fb0ce23f7faa6458d1c6d80c3fa0c3/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:44:06
| Harmonized routes |
|---|
| ORAL |
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 | M012 | openfda.application_number | |
| brand name | Diphenhydramine HCL | openfda.brand_name | |
| generic name | DIPHENHYDRAMINE HCL | openfda.generic_name | |
| manufacturer name | NuCare Pharmaceuticals, Inc. | openfda.manufacturer_name | |
| ndc | package | 66267-081-30 | openfda.package_ndc |
| ndc | product | 66267-081 | openfda.product_ndc |
| ndc11 | package | 66267008130 | derived:openfda.package_ndc |
| rxcui | 1020477 | openfda.rxcui | |
| spl id | 1f98d6d5-cf09-a2bf-e063-6294a90a370b | id | |
| spl set id | 3dbdf020-ca17-1197-e054-00144ff8d46c | set_id | |
| unii | TC2D6JAD40 | 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.