Family Wellness Antiseptic and Pain 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: Family Wellness Antiseptic and Pain Relief
Generic name: BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE
Manufacturer: FRONT PHARMACEUTICAL PLC
Product type: HUMAN OTC DRUG
SPL set ID: cb7fdcde-2bd8-4834-ba4e-4d6fd1512599
SPL ID: 08a19db8-4da9-6529-e063-6394a90a1b4d
Version: 4
Effective date: 2023-10-26
Source export date: 2026-10-27
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/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:17:17

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Family Wellness Antiseptic and Pain Relief	openfda.brand_name
generic name		BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		FRONT PHARMACEUTICAL PLC	openfda.manufacturer_name
ndc	package	69571-007-01	openfda.package_ndc
ndc	product	69571-007	openfda.product_ndc
ndc11	package	69571000701	derived:openfda.package_ndc
spl id		08a19db8-4da9-6529-e063-6394a90a1b4d	id
spl set id		cb7fdcde-2bd8-4834-ba4e-4d6fd1512599	set_id
unii		89Y4M234ES	openfda.unii
unii		057Y626693	openfda.unii
unii		88AYB867L5	openfda.unii
unii		19371312D4	openfda.unii

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 Allergy alert •do not use if allergic to any of the ingredients Do not use •in or near eyes •on large areas of the body Ask a doctor before use if you have •deep or puncture wounds •animal bites •serious burns When using this product •do not use longer than 1 week Stop use and ask a doctor if •condtions last or gets worse •symptoms last for more than 7 days or clear up and come back within a few days •if rash or other allergic reaction occurs

Reported adverse events (FAERS/openFDA)#

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