Anti-itch

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
Anti-itch
Generic name
DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE
Manufacturer
Target Corporation
Product type
HUMAN OTC DRUG
SPL set ID
f444b0a6-2ed3-4236-8206-342150290675
SPL ID
8b820373-a3bd-42f2-aef3-3296d8227d73
Version
2
Effective date
2024-01-17
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 05:52:46
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 product containing diphenhydramine , even one taken by the mouth. Ask a Doctor before use on chicken pox on measles When using this product avoid contact with eyes. Stop use and ask a doctor if conditions worsen or does not improve within 7 days symptoms persist for more than 7 days or clear up and occur agian within a few days

Reported adverse events (FAERS/openFDA)#

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