pain relief acetaminophen pm extra strength

Generic: acetaminophen and diphenhydramine hcl

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief acetaminophen pm extra strength
Generic Name acetaminophen and diphenhydramine hcl
Labeler rite aid corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-2350
Product ID 11822-2350_267b7159-6f61-49de-9cb8-1ec7e4314933
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 118222350
Hyphenated Format 11822-2350

Supplemental Identifiers

RxCUI
1092189
UPC
0011822310697
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 relief acetaminophen pm extra strength (source: ndc)
Generic Name acetaminophen and 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 (11822-2350-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-2350-7)
  • 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-9) / 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (5)

11822-2350-2 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-2) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 11822-2350-5 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 11822-2350-7 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-2350-7) 11822-2350-8 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-8) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 11822-2350-9 1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-9) / 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

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

Linked Drug Pages (1)

Pain Relief Acetaminophen PM Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "267b7159-6f61-49de-9cb8-1ec7e4314933", "openfda": {"upc": ["0011822310697"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["17d27771-a112-474f-9a58-29af0d7e1af3"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-2)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-2350-2", "marketing_start_date": "19940515"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-5)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-2350-5", "marketing_start_date": "19940515"}, {"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (11822-2350-7)", "package_ndc": "11822-2350-7", "marketing_start_date": "19940515"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-8)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-2350-8", "marketing_start_date": "20230403"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (11822-2350-9)  / 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "11822-2350-9", "marketing_start_date": "20230316"}], "brand_name": "Pain Relief Acetaminophen PM Extra Strength", "product_id": "11822-2350_267b7159-6f61-49de-9cb8-1ec7e4314933", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11822-2350", "generic_name": "Acetaminophen and Diphenhydramine HCl", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief Acetaminophen 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"}