pain relief extra strength

Generic: acetaminophen

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief extra strength
Generic Name acetaminophen
Labeler p & l development, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-494
Product ID 59726-494_911f8255-5be5-4012-b398-f2c9e74dc4a8
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2016-03-31
Marketing End 2026-12-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59726494
Hyphenated Format 59726-494

Supplemental Identifiers

RxCUI
198440
UPC
0359726020503
UNII
362O9ITL9D

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 extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-494-05) / 500 TABLET in 1 BOTTLE, PLASTIC
  • 100 TABLET in 1 BOTTLE, PLASTIC (59726-494-10)
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-494-24) / 24 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 BOX (59726-494-50) / 50 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (4)

59726-494-05 1 BOTTLE, PLASTIC in 1 BOX (59726-494-05) / 500 TABLET in 1 BOTTLE, PLASTIC 59726-494-10 100 TABLET in 1 BOTTLE, PLASTIC (59726-494-10) 59726-494-24 1 BOTTLE, PLASTIC in 1 BOX (59726-494-24) / 24 TABLET in 1 BOTTLE, PLASTIC 59726-494-50 1 BOTTLE, PLASTIC in 1 BOX (59726-494-50) / 50 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "911f8255-5be5-4012-b398-f2c9e74dc4a8", "openfda": {"upc": ["0359726020503"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["59eb14a5-40b0-4331-beb5-7166e6cdf411"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-494-05)  / 500 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-494-05", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (59726-494-10)", "package_ndc": "59726-494-10", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-494-24)  / 24 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-494-24", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (59726-494-50)  / 50 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "59726-494-50", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}], "brand_name": "Pain Relief Extra Strength", "product_id": "59726-494_911f8255-5be5-4012-b398-f2c9e74dc4a8", "dosage_form": "TABLET", "product_ndc": "59726-494", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20160331"}