extra strength pain reliever pm

Generic: acetaminophen and diphenhydramine hydrochloride

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

Drug Facts

Product Profile

Brand Name extra strength pain reliever pm
Generic Name acetaminophen and diphenhydramine hydrochloride
Labeler walmart inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
WALMART INC.

Identifiers & Regulatory

Product NDC 79903-053
Product ID 79903-053_495f38a5-3f81-52ec-e063-6394a90abef7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2027-12-31
Marketing Start 2021-01-13

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 79903053
Hyphenated Format 79903-053

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 pain reliever 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
  • 100 TABLET in 1 BOTTLE (79903-053-10)
  • 1 BOTTLE in 1 CARTON (79903-053-24) / 24 TABLET in 1 BOTTLE
source: ndc

Packages (2)

79903-053-10 100 TABLET in 1 BOTTLE (79903-053-10) 79903-053-24 1 BOTTLE in 1 CARTON (79903-053-24) / 24 TABLET in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

EXTRA STRENGTH PAIN RELIEVER PM ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "495f38a5-3f81-52ec-e063-6394a90abef7", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["1092189"], "spl_set_id": ["649e0dd8-ca79-4bf1-9c15-9db9f1d2f5bd"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (79903-053-10)", "package_ndc": "79903-053-10", "marketing_end_date": "20280930", "marketing_start_date": "20210113"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-053-24)  / 24 TABLET in 1 BOTTLE", "package_ndc": "79903-053-24", "marketing_end_date": "20290630", "marketing_start_date": "20210113"}], "brand_name": "EXTRA STRENGTH PAIN RELIEVER PM", "product_id": "79903-053_495f38a5-3f81-52ec-e063-6394a90abef7", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "79903-053", "generic_name": "ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "WALMART INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH PAIN RELIEVER 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": "20210113", "listing_expiration_date": "20271231"}