dual action pain relief

Generic: acetaminophen, ibuprofen

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dual action pain relief
Generic Name acetaminophen, ibuprofen
Labeler target corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 250 mg/1, ibuprofen 125 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-924
Product ID 11673-924_22ecfa46-dbe4-249f-e063-6394a90a70af
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA216994
Listing Expiration 2026-12-31
Marketing Start 2023-07-11

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673924
Hyphenated Format 11673-924

Supplemental Identifiers

RxCUI
2387532
UNII
362O9ITL9D WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

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 dual action pain relief (source: ndc)
Generic Name acetaminophen, ibuprofen (source: ndc)
Application Number ANDA216994 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
  • 125 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-924-75) / 72 TABLET in 1 BOTTLE
source: ndc

Packages (1)

11673-924-75 1 BOTTLE in 1 CARTON (11673-924-75) / 72 TABLET in 1 BOTTLE

Ingredients (2)

acetaminophen (250 mg/1) ibuprofen (125 mg/1)

Linked Drug Pages (1)

Dual Action Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "22ecfa46-dbe4-249f-e063-6394a90a70af", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["e680652b-30d8-6009-e053-2995a90abe29"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-924-75)  / 72 TABLET in 1 BOTTLE", "package_ndc": "11673-924-75", "marketing_start_date": "20230711"}], "brand_name": "Dual Action Pain Relief", "product_id": "11673-924_22ecfa46-dbe4-249f-e063-6394a90a70af", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-924", "generic_name": "Acetaminophen, Ibuprofen", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dual Action Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA216994", "marketing_category": "ANDA", "marketing_start_date": "20230711", "listing_expiration_date": "20261231"}