Cuadriderma

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: Cuadriderma
Generic name: BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE
Manufacturer: ProMex LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4fa99b96-ab4b-4523-82bc-343dbaf39fb6
SPL ID: ea8f2105-b483-4ecb-b1a9-babd58f2e44a
Version: 10
Effective date: 2022-01-25
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:32

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M004	openfda.application_number
brand name		Cuadriderma	openfda.brand_name
generic name		BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		ProMex LLC	openfda.manufacturer_name
ndc	package	58988-1170-1	openfda.package_ndc
ndc	product	58988-1170	openfda.product_ndc
ndc11	package	58988117001	derived:openfda.package_ndc
rxcui		1673566	openfda.rxcui
rxcui		1359350	openfda.rxcui
spl id		ea8f2105-b483-4ecb-b1a9-babd58f2e44a	id
spl set id		4fa99b96-ab4b-4523-82bc-343dbaf39fb6	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 the 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 * condition lasts or gets worse * symptoms last for more than 7 days or clear up and come back within a few days * a rash or other allergic reaction occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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