CVS 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
CVS Itch Relief
Generic name
DIPHENHYDRAMINE HCL, ZINC ACETATE
Manufacturer
CVS
Product type
HUMAN OTC DRUG
SPL set ID
8723e097-296f-784a-e053-2991aa0a552e
SPL ID
4369c991-f8ec-14db-e063-6394a90ad1e1
Version
2
Effective date
2025-11-12
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:29:06
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 · 2 matching rows.

warnings

Warning for external use only

warnings and cautions

For external use only Do not Use on large areas of the body with any other product containing diphenhydramine, even one taken by mouth Ask doctor Before use on chicken pox on measles When using this product do not get into eyes Stop Use and ask physician condition worsens symptoms last 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. Warning for external use only

Reported adverse events (FAERS/openFDA)#

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