Extra Strength Night Time Pain Relief

Generic: Acetaminophen, Diphenhydramine HCl

Labeler: AMERISOURCE BERGEN
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive

Drug Facts

Product Profile

Brand Name Extra Strength Night Time Pain Relief
Generic Name Acetaminophen, Diphenhydramine HCl
Labeler AMERISOURCE BERGEN
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ACETAMINOPHEN 500 mg/1, DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1

Identifiers & Regulatory

Product NDC 46122-707
Product ID 46122-707_3f011b1d-0c88-015b-e063-6394a90a97da
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2022-06-01
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 46122707
Hyphenated Format 46122-707

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 Night Time Pain Relief (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 (46122-707-71) / 50 TABLET, COATED in 1 BOTTLE
  • 100 TABLET, COATED in 1 BOTTLE (46122-707-78)
source: ndc

Packages (2)

46122-707-71 1 BOTTLE in 1 CARTON (46122-707-71) / 50 TABLET, COATED in 1 BOTTLE 46122-707-78 100 TABLET, COATED in 1 BOTTLE (46122-707-78)

Ingredients (2)

ACETAMINOPHEN (500 mg/1) DIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1)

Linked Drug Pages (1)

Extra Strength Night Time Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3f011b1d-0c88-015b-e063-6394a90a97da", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["e5f93e73-9e1e-150a-e053-2995a90a2778"], "manufacturer_name": ["AMERISOURCE BERGEN"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46122-707-71)  / 50 TABLET, COATED in 1 BOTTLE", "package_ndc": "46122-707-71", "marketing_end_date": "20260228", "marketing_start_date": "20220916"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (46122-707-78)", "package_ndc": "46122-707-78", "marketing_end_date": "20260228", "marketing_start_date": "20220920"}], "brand_name": "Extra Strength Night Time Pain Relief", "product_id": "46122-707_3f011b1d-0c88-015b-e063-6394a90a97da", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "46122-707", "generic_name": "Acetaminophen, Diphenhydramine HCl", "labeler_name": "AMERISOURCE BERGEN", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Night Time Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260228", "marketing_start_date": "20220601"}