pain relief pm

Generic: acetaminophen and diphenhydramine hydrochloride

Labeler: harris teeter
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief pm
Generic Name acetaminophen and diphenhydramine hydrochloride
Labeler harris teeter
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
HARRIS TEETER

Identifiers & Regulatory

Product NDC 72036-095
Product ID 72036-095_3596bf4b-c1b3-2dd2-e063-6394a90a6a71
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2011-10-01

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 72036095
Hyphenated Format 72036-095

Supplemental Identifiers

RxCUI
1092189
UPC
0072036987136
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 and diphenhydramine hydrochloride (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 (72036-095-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (72036-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

72036-095-02 1 BOTTLE, PLASTIC in 1 CARTON (72036-095-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 72036-095-03 1 BOTTLE, PLASTIC in 1 CARTON (72036-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC

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": "3596bf4b-c1b3-2dd2-e063-6394a90a6a71", "openfda": {"upc": ["0072036987136"], "unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["0afb6181-d0b1-4845-8230-faabf1b997dc"], "manufacturer_name": ["HARRIS TEETER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72036-095-02)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "72036-095-02", "marketing_start_date": "20111001"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (72036-095-03)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "72036-095-03", "marketing_start_date": "20111001"}], "brand_name": "pain relief PM", "product_id": "72036-095_3596bf4b-c1b3-2dd2-e063-6394a90a6a71", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72036-095", "generic_name": "Acetaminophen and Diphenhydramine Hydrochloride", "labeler_name": "HARRIS TEETER", "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": "20111001", "listing_expiration_date": "20261231"}