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
- Bryant Ranch Prepack
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 59aeb692-2f79-45aa-8e6a-dab77cd3b2f9
- SPL ID
- 93d7cd9d-2520-4547-9afb-4cedbf82c4c4
- Version
- 5
- Effective date
- 2025-03-28
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:57:31
| 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 | Bryant Ranch Prepack | openfda.manufacturer_name | |
| ndc | package | 71335-0352-2 | openfda.package_ndc |
| ndc | package | 71335-0352-5 | openfda.package_ndc |
| ndc | package | 71335-0352-6 | openfda.package_ndc |
| ndc | package | 71335-0352-8 | openfda.package_ndc |
| ndc | package | 71335-0352-9 | openfda.package_ndc |
| ndc | package | 71335-0352-7 | openfda.package_ndc |
| ndc | package | 71335-0352-0 | openfda.package_ndc |
| ndc | package | 71335-0352-4 | openfda.package_ndc |
| ndc | package | 71335-0352-3 | openfda.package_ndc |
| ndc | package | 71335-0352-1 | openfda.package_ndc |
| ndc | product | 71335-0352 | openfda.product_ndc |
| ndc11 | package | 71335035209 | derived:openfda.package_ndc |
| ndc11 | package | 71335035205 | derived:openfda.package_ndc |
| ndc11 | package | 71335035203 | derived:openfda.package_ndc |
| ndc11 | package | 71335035207 | derived:openfda.package_ndc |
| ndc11 | package | 71335035208 | derived:openfda.package_ndc |
| ndc11 | package | 71335035200 | derived:openfda.package_ndc |
| ndc11 | package | 71335035206 | derived:openfda.package_ndc |
| ndc11 | package | 71335035201 | derived:openfda.package_ndc |
| ndc11 | package | 71335035202 | derived:openfda.package_ndc |
| ndc11 | package | 71335035204 | derived:openfda.package_ndc |
| rxcui | 1049909 | openfda.rxcui | |
| spl id | 93d7cd9d-2520-4547-9afb-4cedbf82c4c4 | id | |
| spl set id | 59aeb692-2f79-45aa-8e6a-dab77cd3b2f9 | 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.