FDA label 41efb43b-576e-4e7c-9fb4-e61d5a6d2fd5

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)

SPL set ID
f0a4598e-df39-4f0a-9c52-98af58b9718a
SPL ID
41efb43b-576e-4e7c-9fb4-e61d5a6d2fd5
Version
1
Effective date
2017-01-20
Source export date
2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:06:59

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 For external use only. Do not use • on large areas of the body • with any other product containing diphenhydramine, even one taken by mouth When using this product • avoid contact with the eyes S top use and ask doctor if • condition gets worse • symptoms last more than 7 days • symptoms clear up and occur again in a few days.

Reported adverse events (FAERS/openFDA)#

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