Menstrual Bloat Relief

Product NDC
79903-425
11-digit product format
799030425
Labeler code
79903
Product ID
79903-425_6bcbbfe8-6328-4442-8b41-6a8c3b71859a
Type
HUMAN OTC DRUG
Nonproprietary name
Pamabrom
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
WALMART INC.
Application
M027
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-04-07
Substance
PAMABROM
Active strength
50 mg/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Menstrual Bloat Relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PAMABROM50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiUA8U0KJM72
Rxcui199158

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79903-425-30Menstrual Bloat Relief30 in 1 BOTTLE, PLASTICTABLET, FILM COATED302
79903-425-30Menstrual Bloat Relief1 in 1 CARTONTABLET, FILM COATED12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199158pamabrom 50 MG Oral TabletPSN6479b326-8b20-401e-8224-a05f6d7dce2e2
199158pamabrom 50 MG Oral TabletSCD6479b326-8b20-401e-8224-a05f6d7dce2e2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
79903-425-30799030425301 BOTTLE, PLASTIC in 1 CARTON (79903-425-30) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2026-04-07NoNoCurrent