extra strength pm pain medicine

Generic: acetaminophen, diphenhydramine hcl

Labeler: amerisource bergen
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength pm pain medicine
Generic Name acetaminophen, diphenhydramine hcl
Labeler amerisource bergen
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
Amerisource Bergen

Identifiers & Regulatory

Product NDC 46122-799
Product ID 46122-799_23fbc0e1-3e01-acb4-e063-6394a90ac9db
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-10-01

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 46122799
Hyphenated Format 46122-799

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 extra strength pm pain medicine (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 (46122-799-69) / 50 TABLET in 1 BOTTLE
  • 100 TABLET in 1 BOTTLE (46122-799-70)
source: ndc

Packages (2)

46122-799-69 1 BOTTLE in 1 CARTON (46122-799-69) / 50 TABLET in 1 BOTTLE 46122-799-70 100 TABLET in 1 BOTTLE (46122-799-70)

Ingredients (2)

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

Linked Drug Pages (1)

Extra Strength PM Pain Medicine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "23fbc0e1-3e01-acb4-e063-6394a90ac9db", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["23fbda2b-885b-ce00-e063-6294a90a586e"], "manufacturer_name": ["Amerisource Bergen"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46122-799-69)  / 50 TABLET in 1 BOTTLE", "package_ndc": "46122-799-69", "marketing_start_date": "20241001"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (46122-799-70)", "package_ndc": "46122-799-70", "marketing_start_date": "20241001"}], "brand_name": "Extra Strength PM Pain Medicine", "product_id": "46122-799_23fbc0e1-3e01-acb4-e063-6394a90ac9db", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "46122-799", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "Amerisource Bergen", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength PM Pain Medicine", "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": "20241001", "listing_expiration_date": "20261231"}