pain reliever pm extra strength

Generic: acetaminophen, diphenhydramine hcl

Labeler: salado sales, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain reliever pm extra strength
Generic Name acetaminophen, diphenhydramine hcl
Labeler salado sales, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, diphenhydramine hydrochloride 25 mg/1

Manufacturer
Salado Sales, Inc.

Identifiers & Regulatory

Product NDC 57243-235
Product ID 57243-235_c3e081b6-59d1-472c-a56f-579cf8b0e222
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1994-05-15

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57243235
Hyphenated Format 57243-235

Supplemental Identifiers

RxCUI
1092189
UPC
0761706160220
UNII
362O9ITL9D TC2D6JAD40

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name pain reliever pm extra strength (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (57243-235-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

57243-235-15 1 BOTTLE, PLASTIC in 1 CARTON (57243-235-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

acetaminophen (500 mg/1) diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Pain Reliever PM Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c3e081b6-59d1-472c-a56f-579cf8b0e222", "openfda": {"upc": ["0761706160220"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["aef30709-f33d-48ff-b2d4-0639ffbd1ffd"], "manufacturer_name": ["Salado Sales, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (57243-235-15)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "57243-235-15", "marketing_start_date": "19940515"}], "brand_name": "Pain Reliever PM Extra Strength", "product_id": "57243-235_c3e081b6-59d1-472c-a56f-579cf8b0e222", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "57243-235", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Salado Sales, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever PM", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19940515", "listing_expiration_date": "20261231"}