GoodSense 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
GoodSense Anti-Itch
Generic name
DIPHENHYDRAMINE HCL, ZINC ACETATE
Manufacturer
Geiss, Destin & Dunn, Inc
Product type
HUMAN OTC DRUG
SPL set ID
2f38bdfc-6135-1b8a-e063-6294a90a6703
SPL ID
2f38bdfc-6134-1b8a-e063-6294a90a6703
Version
1
Effective date
2025-02-28
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:45:43
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

Flammable . Keep away from excessive heat or open flame. For external use only . Do not use on chicken pox, on large areas of the body, with any other products containing diphenhydramine, even one take by mouth. When using this product avoid spraying in eyes. Stop use and ask a doctor if the condition worsens, rash or irritation develops and lasts for more than 7 days or clears up and occurs again within a few days.

Reported adverse events (FAERS/openFDA)#

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