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
GLYCERIN, PHENYLEPHRINE HYDROCHLORIDE, PRAMOXINE HYDROCHLORIDE, PETROLATUM
Manufacturer
Zhejiang Jingwei Pharmaceutical Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
fde9cd90-d63c-4058-b46e-511fecea36ec
SPL ID
08835b51-a1a6-985b-e063-6294a90a14c9
Version
3
Effective date
2023-10-24
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:46:35
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. When using this product -do not put this product into the rectum by using fingers or any mechanical device or applicator -do not exceed recommended daily dosage unless directed by a doctor Ask a doctor before use if you have -heart disease -high blood pressure -thyroid disease -diabetes -trouble urinating due to an enlarged prostate gland presently taking a prescription Ask a doctor or pharmacist before use if you are drug for high blood pressure. Stop use and ask a doctor if -bleeding occurs -condition worsens or does not improve within 7 days. -if the symptoms being treated do not subside or if redness, irritation, swelling, pain or other symptoms develop or increase. Some people can develop allergic reactions to ingredients in this product. , ask a health professional before use. If pregnant or breast-feeding

Reported adverse events (FAERS/openFDA)#

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