SUNMARK TRIPLE ANTIBIOTIC PLUS 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: SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF
Generic name: POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE
Manufacturer: A-S Medication Solutions
Product type: HUMAN OTC DRUG
SPL set ID: 01131ba6-6d5b-4710-bec3-ba1769c08c79
SPL ID: 8ccae7c4-e443-4cec-a31d-764334293b65
Version: 2
Effective date: 2024-10-22
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:29:43

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF	openfda.brand_name
generic name		POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		A-S Medication Solutions	openfda.manufacturer_name
ndc	package	50090-6172-0	openfda.package_ndc
ndc	product	50090-6172	openfda.product_ndc
ndc11	package	50090617200	derived:openfda.package_ndc
rxcui		1359350	openfda.rxcui
spl id		8ccae7c4-e443-4cec-a31d-764334293b65	id
spl set id		01131ba6-6d5b-4710-bec3-ba1769c08c79	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 Do not use if you are allergic to any of the ingredients Ask a doctor before use if you have deep or puncture wounds animal bites serious burns When using this product do not use in the eyes do not apply over large areas of the body Stop use and ask a doctor if you need to use for more than 1 week condition persists or gets worse symptoms persist for more than 1 week or clear up and occur again within a few days rash or other allergic reaction develops Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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