Family Wellness

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
Family Wellness
Generic name
DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE
Manufacturer
FRONT PHARMACEUTICAL PLC
Product type
HUMAN OTC DRUG
SPL set ID
fde2069b-344e-46da-bb95-c5113e0f35d6
SPL ID
08a16eed-ba21-b1fa-e063-6294a90a6615
Version
4
Effective date
2023-10-26
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:17:53
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 •avoid contact with eyes When using this product Ask a doctor before use •on chicken pox •on measles Stop use and ask a doctor if over large areas of the body with any other product containing diphenhydramine including those taken orally symptoms last for more than 7 days the condition gets worse symptoms clear up and then occur again within a few days

Reported adverse events (FAERS/openFDA)#

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