pain relief pm extra strength

Generic: acetaminophen, diphenhydramine hcl

Labeler: publix super markets inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief pm extra strength
Generic Name acetaminophen, diphenhydramine hcl
Labeler publix super markets inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Publix Super Markets Inc

Identifiers & Regulatory

Product NDC 56062-437
Product ID 56062-437_30a3e4c3-88bf-4126-80ff-f63f50e90ba1
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 1993-09-22

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 56062437
Hyphenated Format 56062-437

Supplemental Identifiers

RxCUI
1092189
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 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 in 1 CARTON (56062-437-71) / 50 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (56062-437-78) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (2)

56062-437-71 1 BOTTLE in 1 CARTON (56062-437-71) / 50 TABLET, FILM COATED in 1 BOTTLE 56062-437-78 1 BOTTLE in 1 CARTON (56062-437-78) / 100 TABLET, FILM COATED in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

pain relief pm extra strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "30a3e4c3-88bf-4126-80ff-f63f50e90ba1", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["42d271b7-b45f-4497-8de2-4e05b4bebfa9"], "manufacturer_name": ["Publix Super Markets Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-437-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-437-71", "marketing_start_date": "19930922"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-437-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-437-78", "marketing_start_date": "19930922"}], "brand_name": "pain relief pm extra strength", "product_id": "56062-437_30a3e4c3-88bf-4126-80ff-f63f50e90ba1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "56062-437", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Publix Super Markets Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "pain relief 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": "19930922", "listing_expiration_date": "20261231"}