PAMABROM capsule, liquid filled

Pamabrom by

Drug Labeling and Warnings

Pamabrom by is a Otc medication manufactured, distributed, or labeled by WALGREENS CO.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Pamabrom 50mg

PURPOSE

Diuretic

INACTIVE INGREDIENT

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

DOSAGE & ADMINISTRATION

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

For the relief of

temporary water wieght gain

bloating

swelling

full feling associated with the premenstrual and menstrual periods

WARNINGS

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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OVERDOSAGE

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAMABROM 
pamabrom capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0795
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PAMABROM (UNII: UA8U0KJM72) (BROMOTHEOPHYLLINE - UNII:FZG87K1MQ6)	PAMABROM	50 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
SORBITOL (UNII: 506T60A25R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
POVIDONE K30 (UNII: U725QWY32X)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	blue	Score	no score
Shape	OVAL (Oblong)	Size	14mm
Flavor		Imprint Code	795
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0795-84	48 in 1 BOTTLE; Type 0: Not a Combination Product	11/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/24/2020

Labeler - WALGREENS CO. (008965063)