Allergy 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 (canonical bytes are SHA-256 checked before publication)

Brand name
Allergy Relief
Generic name
DIPHENHYDRAMINE HCL
Manufacturer
LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION
Product type
HUMAN OTC DRUG
SPL set ID
2a46ea9b-29e9-5197-e063-6394a90abc73
SPL ID
4745dfbc-e512-5953-e063-6394a90a3b26
Version
2
Effective date
2025-12-31
Source export date
2026-11-06
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:16:06
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use with any other product conatining diphenhydramine, including one used on the skin to make a child sleepy Ask a doctor before use if you have a breathing problem such as chronic bronchitis glaucoma Ask a doctor or pharmacist before use if the child is taking sedatives or tranquilizers. When using this product do not exceed recommended dose excitability may occur, especially in children marked drowsiness may occur sedatives, and tranquilizers may increase drowsiness

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.