DIUREX MAX- pamabrom tablet, film coated 
Alva-Amco Pharmacal Companies, Inc.

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Diurex Max

Active ingredient (in each caplet)

Pamabrom, 50 mg

Purpose


Diuretic

Uses

For the relief of

associated with the premenstrual and menstrual periods.

Warnings


Ask a doctor or pharmacist before use if you are taking any other medications.

Stop use and ask a doctor if symptoms last more than ten consecutive days.

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children.  In case of overdose, get medical help or contact a poison control center right away.

Directions

Other information

Calcium content: 160 mg/pill. **Contents sealed: Each DIUREX Max, light blue colored, oval shaped pill bears the identifying mark "ALVA" plus a "1" on the pill's reverse side and is sealed in a clear plastic blister with a foil backing. Do not use if seal appears broken or if product contents do not match product description. NOTE: The appearance of golden tinted urine which may occur after taking Diurex Water Pills is a normal and temporary effect. You may report serious side effects to the phone number provided under Questions? below.

Inactive ingredients

Calcium sulfate dihydrate, croscarmellose sodium, dicalcium phosphate, FDC Blue No. 1, hypromellose, magnesium stearate, mineral oil, polyethylene glycol, potassium gluconate, riboflavin, sodium lauryl sulfate, stearic acid, talc and titanium dioxide.

Questions?  1-800-792-2582

Diurex Max Spanish Drug Facts

DiurexMaxPDP

DIUREX  MAX
pamabrom tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52389-249
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PAMABROM (UNII: UA8U0KJM72) (BROMOTHEOPHYLLINE - UNII:FZG87K1MQ6) PAMABROM50 mg
Inactive Ingredients
Ingredient NameStrength
CALCIUM SULFATE DIHYDRATE (UNII: 4846Q921YM)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POTASSIUM GLUCONATE (UNII: 12H3K5QKN9)  
RIBOFLAVIN (UNII: TLM2976OFR)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorblueScoreno score
ShapeOVALSize15mm
FlavorImprint Code ALVA;1
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52389-249-201 in 1 CARTON07/18/200604/18/2011
130 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:52389-249-401 in 1 CARTON10/01/201503/31/2019
240 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:52389-249-241 in 1 CARTON04/18/2011
324 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:52389-249-482 in 1 CARTON07/18/2013
424 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:52389-249-162 in 1 CARTON04/18/201105/31/2019
58 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC:52389-249-104 in 1 CARTON11/10/2017
610 in 1 BLISTER PACK; Type 0: Not a Combination Product
7NDC:52389-249-723 in 1 CARTON06/12/2018
724 in 1 BLISTER PACK; Type 0: Not a Combination Product
8NDC:52389-249-303 in 1 CARTON07/12/2021
810 in 1 BLISTER PACK; Type 0: Not a Combination Product
9NDC:52389-249-505 in 1 CARTON07/18/2022
910 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02712/20/1995
Labeler - Alva-Amco Pharmacal Companies, Inc. (042074856)

Revised: 11/2023
Document Id: 0b4d8159-e944-7cd4-e063-6394a90a49bc
Set id: 37dfece3-d570-4ab2-ba95-af6eb1f3acd4
Version: 12
Effective Time: 20231129
 
Alva-Amco Pharmacal Companies, Inc.