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 (canonical bytes are SHA-256 checked before publication)

Brand name
Itch Relief
Generic name
DIPHENHYDRAMINE HYDROCHLORIDE
Manufacturer
Safetec of America, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
4f4c801b-d894-4fa3-b024-6ca41a5f2a95
SPL ID
109674e0-ef83-5844-e063-6394a90ae6b8
Version
3
Effective date
2024-02-04
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:35:48
Harmonized routes table
Harmonized routes
TOPICAL

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 products using diphenhydramine hydrochloride, even one taken by mouth Ask a doctor before use on chicken pox on measles When using this product avoid contact with the eyes Stop use and ask doctor if condition worsens symptoms persist more than 7 days or clear up and occur again within a few days Keep out of reach of children If swallowed, get medical help or contact a poison control center right away.

Reported adverse events (FAERS/openFDA)#

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