AX Pharmaceutical Corp

Manufacturer: AX Pharmaceutical Corp
Effective date: 2018-10-11
Label type: BULK INGREDIENT
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:49:11

Label at a glance#

ProductAX Pharmaceutical Corp

Active ingredientPAROMOMYCIN SULFATE

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62157-702-01	AX Pharmaceutical Corp	500 g in 1 JAR	POWDER	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62157-702	AX PHARMACEUTICAL CORP (PAROMOMYCIN SULFATE) POWDER [AX PHARMACEUTICAL CORP]	1	1 package rows	20190112_ce855ccf-2354-47df-ad45-7e7076b0d469.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

AX Pharmaceutical Corp
PAROMOMYCIN SULFATE
PAROMOMYCIN
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62157-702	62157-702-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PAROMOMYCIN SULFATE	845NU6GJPS	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Humatin	PAROMOMYCIN SULFATE	Waylis Therapeutics LLC	a725f022-ec3c-430d-8021-96c861b9893c	2025-11-13	Adverse reactions	Name fallback generic name: PAROMOMYCIN SULFATE

Reported adverse events (FAERS/openFDA)#

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