Pamabrom

Manufacturer
WALGREENS CO.
Effective date
2024-01-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:07:15

Label at a glance#

ProductPamabrom
Active ingredientPAMABROM
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Pamabrom 50mg

OTC - PURPOSE SECTION

Diuretic

INACTIVE INGREDIENT SECTION

FD&C Blue#1, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol and titanium dioxide

DOSAGE & ADMINISTRATION SECTION

Read all package direction and warnings before use.

Use only as directed.

Adults: One(1) softgel capsule after breakfast with a full glass of water.

Dose may be repeated after 6 hours, not to exceed four (4) softgel capsules in 24 hours.

Start taking 5 or 6 days before onset of period and continue until desired relief is obtained or end of period.

Drink 6 to 8 glasses of water daily.

For use by normally healthy adults only

Persons under 18 years of age should use only as directed by a doctor.

INDICATIONS & USAGE SECTION

For the relief of

temporary water wieght gain

bloating

swelling

full feling associated with the premenstrual and menstrual periods

WARNINGS SECTION

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

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

If pregnant or breast-feeding, 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away.

OTHER SAFETY INFORMATION

Contents sealed: Each clear translucent blue-colored, oval shaped Diuretic softgel capsule bears the identifying mark "795".

Contents packaged ina bottle with a safety seal under cap. Do not use if seal appears broken.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

diureticdiuretic

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
832080pamabrom 50 MG Oral CapsulePSN2
832080pamabrom 50 MG Oral CapsuleSCD2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0795-84Pamabrom48 in 1 BOTTLECAPSULE, LIQUID FILLED482

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0795PAMABROM CAPSULE, LIQUID FILLED [WALGREENS CO.]2Current NDC, Legacy NDC, 1 package rows20240116_b4e11a36-94dc-274d-e053-2a95a90ab894.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-07950363-0795-84

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PamabromPAMABROMWALGREENS CO.b4e11a36-94dc-274d-e053-2a95a90ab8942024-01-15WarningsExact identifier
ndc (package): 0363-0795-84
ndc (product): 0363-0795
ndc11 (package): 00363079584
spl id: bb01ae5b-4059-46e4-84b9-f2e605261761
spl set id: b4e11a36-94dc-274d-e053-2a95a90ab894

Reported adverse events (FAERS/openFDA)#

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