Anti-Itch Cream

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 Cream
Generic name
DIPHENHYDRAMINE HYDROCHLORIDE 2%, ZINC ACETATE 0.1%
Manufacturer
Chain Drug Marketing Association Inc.
Product type
HUMAN OTC DRUG
SPL set ID
2b48cb2f-e6bf-f9de-e063-6394a90a42d4
SPL ID
2b48d177-e250-2621-e063-6394a90ae278
Version
1
Effective date
2025-01-09
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:16:03
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 or with any other product containing diphenhydramine, even one taken by mouth Ask a doctor before use on chicken pox or measles When using this product avoid contact with eyes Stop use and ask a doctor if Conditions worsen or do not improve within 7 days Symptoms persist for more than 7 days or clear up and occur again within a few days

Reported adverse events (FAERS/openFDA)#

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