pain relief pm

Generic: acetaminophen, diphenhydramine hcl

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

Drug Facts

Product Profile

Brand Name pain relief pm
Generic Name acetaminophen, diphenhydramine hcl
Labeler dolgencorp, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
DOLGENCORP, INC.

Identifiers & Regulatory

Product NDC 55910-834
Product ID 55910-834_0d05f2d6-747e-27e1-e063-6394a90a1797
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2023-12-25

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 55910834
Hyphenated Format 55910-834

Supplemental Identifiers

RxCUI
1092189
UPC
0355910834055 0355910834017
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 pm (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 in 1 CARTON (55910-834-01) / 100 TABLET in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (55910-834-05) / 50 TABLET in 1 BOTTLE
source: ndc

Packages (2)

55910-834-01 1 BOTTLE in 1 CARTON (55910-834-01) / 100 TABLET in 1 BOTTLE 55910-834-05 1 BOTTLE in 1 CARTON (55910-834-05) / 50 TABLET in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

Pain Relief PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0d05f2d6-747e-27e1-e063-6394a90a1797", "openfda": {"upc": ["0355910834055", "0355910834017"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["06553550-5685-f3c3-e063-6394a90aef07"], "manufacturer_name": ["DOLGENCORP, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-834-01)  / 100 TABLET in 1 BOTTLE", "package_ndc": "55910-834-01", "marketing_start_date": "20231225"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-834-05)  / 50 TABLET in 1 BOTTLE", "package_ndc": "55910-834-05", "marketing_start_date": "20231225"}], "brand_name": "Pain Relief PM", "product_id": "55910-834_0d05f2d6-747e-27e1-e063-6394a90a1797", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55910-834", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "DOLGENCORP, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief 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": "20231225", "listing_expiration_date": "20261231"}