pain relief acetaminophen pm

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
Generic Name acetaminophen and diphenhydramine hcl
Labeler rite aid corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-0556
Product ID 11822-0556_d7058f45-483c-4b4d-a1ce-41c52c43a654
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2007-12-17

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 118220556
Hyphenated Format 11822-0556

Supplemental Identifiers

RxCUI
1092189
UPC
0011822606011
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 (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
  • 80 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0556-1)
source: ndc

Packages (1)

11822-0556-1 80 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0556-1)

Ingredients (2)

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

Linked Drug Pages (1)

Pain Relief Acetaminophen PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d7058f45-483c-4b4d-a1ce-41c52c43a654", "openfda": {"upc": ["0011822606011"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["f77f0120-4042-4b11-ba9c-cd35e1cd0bee"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET, COATED in 1 BOTTLE, PLASTIC (11822-0556-1)", "package_ndc": "11822-0556-1", "marketing_start_date": "20071217"}], "brand_name": "Pain Relief Acetaminophen PM", "product_id": "11822-0556_d7058f45-483c-4b4d-a1ce-41c52c43a654", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11822-0556", "generic_name": "Acetaminophen and Diphenhydramine HCl", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief Acetaminophen PM", "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": "20071217", "listing_expiration_date": "20271231"}