Medi First Plus PMS Relief

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Medi First Plus PMS Relief
Generic name: ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE
Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: e84007e7-498d-4662-e053-2995a90ad4de
SPL ID: 3e5d5132-9c04-1a98-e063-6394a90a6a9c
Version: 5
Effective date: 2025-09-09
Source export date: 2026-11-06
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:52:03

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M027	openfda.application_number
brand name		Medi First PMS Relief	openfda.brand_name
brand name		Medi First Plus PMS Relief	openfda.brand_name
generic name		ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-723-36	openfda.package_ndc
ndc	package	47682-823-80	openfda.package_ndc
ndc	package	47682-723-80	openfda.package_ndc
ndc	package	47682-823-36	openfda.package_ndc
ndc	package	47682-823-99	openfda.package_ndc
ndc	product	47682-723	openfda.product_ndc
ndc	product	47682-823	openfda.product_ndc
ndc11	package	47682072336	derived:openfda.package_ndc
ndc11	package	47682082380	derived:openfda.package_ndc
ndc11	package	47682072380	derived:openfda.package_ndc
ndc11	package	47682082336	derived:openfda.package_ndc
ndc11	package	47682082399	derived:openfda.package_ndc
rxcui		1052637	openfda.rxcui
spl id		3e5d5132-9c04-1a98-e063-6394a90a6a9c	id
spl set id		e84007e7-498d-4662-e053-2995a90ad4de	set_id
unii		R35D29L3ZA	openfda.unii
unii		UA8U0KJM72	openfda.unii
unii		362O9ITL9D	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take ■ more than 4,000 mg of acetaminophen in 24 hours ■ with other drugs containing acetaminophen ■ 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: ■ skin reddening ■ blisters ■ rash If a skin reaction occurs, stop use and seek medical help right away.

Reported adverse events (FAERS/openFDA)#

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