Diurex

Manufacturer: Kobayashi Healthcare International, Inc. | Kobayashi American Manufacturing, LLC
Effective date: 2025-05-07
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 01:00:39

Label at a glance#

ProductDiurex Max

Active ingredientPAMABROM

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
199158	pamabrom 50 MG Oral Tablet	PSN	7
199158	pamabrom 50 MG Oral Tablet	SCD	7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52389-349-16	DiurexMax	8 in 1 BLISTER PACK	TABLET, FILM COATED	8		7
52389-349-16	DiurexMax	2 in 1 CARTON	TABLET, FILM COATED	2		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52389-349	DIUREX MAX (PAMABROM) TABLET, FILM COATED [KOBAYASHI HEALTHCARE INTERNATIONAL, INC.]	7	2 package rows	20250509_874aa629-1330-0c30-e053-2a95a90ac888.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

Diurex Max
Pamabrom
CROSCARMELLOSE SODIUM
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
FD&C BLUE NO. 1
HYPROMELLOSES
MAGNESIUM STEARATE
LIGHT MINERAL OIL
POLYETHYLENE GLYCOL 400
CALCIUM SULFATE DIHYDRATE
POTASSIUM GLUCONATE
RIBOFLAVIN
SODIUM LAURYL SULFATE
STEARIC ACID
TITANIUM DIOXIDE
BROMOTHEOPHYLLINE
TALC

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52389-349	52389-349-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATE	O7TSZ97GEP	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
HYPROMELLOSES	3NXW29V3WO	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
LIGHT MINERAL OIL	N6K5787QVP	IACT
POLYETHYLENE GLYCOL 400	B697894SGQ	IACT
CALCIUM SULFATE DIHYDRATE	4846Q921YM	IACT
POTASSIUM GLUCONATE	12H3K5QKN9	IACT
RIBOFLAVIN	TLM2976OFR	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
STEARIC ACID	4ELV7Z65AP	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
PAMABROM	UA8U0KJM72	ACTIB
TALC	7SEV7J4R1U	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
347a7341-b8d5-cdb3-e063-6394a90aff60			874aa629-1330-0c30-e053-2a95a90ac888	2025-05-07		Exact identifier spl id: 347a7341-b8d5-cdb3-e063-6394a90aff60 spl set id: 874aa629-1330-0c30-e053-2a95a90ac888

Reported adverse events (FAERS/openFDA)#

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