PENTREXCILINA 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: PENTREXCILINA TRIPLE ANTIBIOTIC PLUS PAIN RELIEF
Generic name: BACITRACIN, NEOMYCIN, POLYMYXIN B, PRAMOXINE
Manufacturer: OPMX LLC
Product type: HUMAN OTC DRUG
SPL set ID: 7c0d3cdf-af50-4a65-a01b-a33510feeb94
SPL ID: 18ac00d7-fdc6-65b1-e063-6394a90ac204
Version: 3
Effective date: 2024-05-17
Source export date: 2026-10-12
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:43:39

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		PENTREXCILINA TRIPLE ANTIBIOTIC PLUS PAIN RELIEF	openfda.brand_name
generic name		BACITRACIN, NEOMYCIN, POLYMYXIN B, PRAMOXINE	openfda.generic_name
manufacturer name		OPMX LLC	openfda.manufacturer_name
ndc	package	69729-616-61	openfda.package_ndc
ndc	package	69729-616-01	openfda.package_ndc
ndc	product	69729-616	openfda.product_ndc
ndc11	package	69729061661	derived:openfda.package_ndc
ndc11	package	69729061601	derived:openfda.package_ndc
rxcui		2055751	openfda.rxcui
spl id		18ac00d7-fdc6-65b1-e063-6394a90ac204	id
spl set id		7c0d3cdf-af50-4a65-a01b-a33510feeb94	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 IN THE EYES IF YOU ARE ALLERGIC TO ANY OF THE INGREDIENTS OVER LARGE AREAS OF THE BODY LONGER THAN 1 WEEK UNLESS DIRECTED BY A DOCTOR ASK A DOCTOR BEFORE USE IN CASE OF DEEP OR PUNCTURE WOUNDS ANIMAL BITES OR SERIOUS BURNS

Reported adverse events (FAERS/openFDA)#

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