Pamprin

Manufacturer
Focus Consumer Healthcare, LLC
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:29:09

Label at a glance#

ProductPamprin Bloat
Active ingredientPAMABROM
Label structure10 sections

Indications and uses

For the temporary relief of bloating water-weight gain swelling full feeling associated with the premenstrual and menstrual periods.

Dosage and administration

do not take more than the recommended dose adults and children 12 years and older: take 1 caplet with water repeated every 6 hours, as needed do not exceed 4 caplets per day children under 12 years: consult a doctor

Label contents#

Full prescribing information#

Active ingredient (in each caplet)

OTC - ACTIVE INGREDIENT SECTION

Pamabrom 50 mg

Purpose

OTC - PURPOSE SECTION



Diuretic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of

  • bloating
  • water-weight gain
  • swelling
  • full feeling

associated with the premenstrual and menstrual periods.

Do not use

OTC - DO NOT USE SECTION

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not take more than the recommended dose
  • adults and children 12 years and older:
  • take 1 caplet with water
  • repeated every 6 hours, as needed
  • do not exceed 4 caplets per day
  • children under 12 years: consult a doctor

Other information

INFORMATION FOR PATIENTS SECTION

Each caplet contains: 170 mg of Calcium

Inactive ingredients

INACTIVE INGREDIENT SECTION

calcium sulfate dihydrate, croscarmellose sodium, dibasic calcium phosphate dihydrate, FDC Blue #1 lake, hypromellose, magnesium stearate, mineral oil, polyethylene glycol, potassium gluconate, riboflavin, sodium lauryl sulfate, stearic acid, talc, titanium dioxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
199158pamabrom 50 MG Oral TabletPSN1
199158pamabrom 50 MG Oral TabletSCD1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71687-3009-1PamprinBloat1 in 1 CARTONTABLET, FILM COATED11
71687-3009-1PamprinBloat30 in 1 BOTTLETABLET, FILM COATED301

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71687-300971687-3009-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
Pamprin BloatPAMABROMFocus Consumer Healthcare, LLC42f1846d-2d57-5221-e063-6394a90a3a9f2025-12-31WarningsExact identifier
ndc (package): 71687-3009-1
ndc (product): 71687-3009
ndc11 (package): 71687300901
spl id: 42f18430-4323-4a63-e063-6394a90a0382
spl set id: 42f1846d-2d57-5221-e063-6394a90a3a9f

Reported adverse events (FAERS/openFDA)#

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