pain relief pm

Generic: acetaminophen, aspirin, diphenhydramine citrate

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief pm
Generic Name acetaminophen, aspirin, diphenhydramine citrate
Labeler cvs pharmacy
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 250 mg/1, aspirin 250 mg/1, diphenhydramine citrate 38 mg/1

Manufacturer
CVS Pharmacy

Identifiers & Regulatory

Product NDC 59779-894
Product ID 59779-894_c881bdd1-5613-4adf-a0df-79f6e1ca0129
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2016-08-31
Marketing End 2027-06-30

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc] platelet aggregation inhibitor [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]
Physiologic Effect
decreased prostaglandin production [pe] decreased platelet aggregation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59779894
Hyphenated Format 59779-894

Supplemental Identifiers

RxCUI
1593110
UPC
0050428421772
UNII
362O9ITL9D R16CO5Y76E 4OD433S209
NUI
N0000000160 N0000008836 M0001335 N0000175722 N0000175578 N0000008832

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, aspirin, diphenhydramine citrate (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
  • 38 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (59779-894-12) / 100 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (1)

59779-894-12 1 BOTTLE in 1 CARTON (59779-894-12) / 100 TABLET, FILM COATED in 1 BOTTLE

Ingredients (3)

acetaminophen (250 mg/1) aspirin (250 mg/1) diphenhydramine citrate (38 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": "c881bdd1-5613-4adf-a0df-79f6e1ca0129", "openfda": {"nui": ["N0000000160", "N0000008836", "M0001335", "N0000175722", "N0000175578", "N0000008832"], "upc": ["0050428421772"], "unii": ["362O9ITL9D", "R16CO5Y76E", "4OD433S209"], "rxcui": ["1593110"], "spl_set_id": ["ddd78b28-6e10-4708-bed1-8aea087b3d82"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_pe": ["Decreased Prostaglandin Production [PE]", "Decreased Platelet Aggregation [PE]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59779-894-12)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "59779-894-12", "marketing_end_date": "20270630", "marketing_start_date": "20160831"}], "brand_name": "Pain Relief PM", "product_id": "59779-894_c881bdd1-5613-4adf-a0df-79f6e1ca0129", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "Decreased Prostaglandin Production [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "Platelet Aggregation Inhibitor [EPC]"], "product_ndc": "59779-894", "generic_name": "Acetaminophen, Aspirin, Diphenhydramine citrate", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief PM", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "ASPIRIN", "strength": "250 mg/1"}, {"name": "DIPHENHYDRAMINE CITRATE", "strength": "38 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270630", "marketing_start_date": "20160831"}