extra strength no-pain

Generic: acetaminophen

Labeler: safrel pharmaceuticals, llc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength no-pain
Generic Name acetaminophen
Labeler safrel pharmaceuticals, llc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
Safrel Pharmaceuticals, LLC.

Identifiers & Regulatory

Product NDC 71309-001
Product ID 71309-001_3371e8dc-ae55-9a65-e063-6394a90aeaac
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2017-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71309001
Hyphenated Format 71309-001

Supplemental Identifiers

RxCUI
198440
UPC
0371309001051
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 extra strength no-pain (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
  • 500 TABLET in 1 BOTTLE (71309-001-05)
  • 1 BOTTLE in 1 CARTON (71309-001-40) / 40 TABLET in 1 BOTTLE
source: ndc

Packages (2)

71309-001-05 500 TABLET in 1 BOTTLE (71309-001-05) 71309-001-40 1 BOTTLE in 1 CARTON (71309-001-40) / 40 TABLET in 1 BOTTLE

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Extra Strength No-Pain ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3371e8dc-ae55-9a65-e063-6394a90aeaac", "openfda": {"upc": ["0371309001051"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["873f01dd-0701-5fd3-e053-2a95a90a6463"], "manufacturer_name": ["Safrel Pharmaceuticals, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71309-001-05)", "package_ndc": "71309-001-05", "marketing_start_date": "20170731"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (71309-001-40)  / 40 TABLET in 1 BOTTLE", "package_ndc": "71309-001-40", "marketing_start_date": "20170731"}], "brand_name": "Extra Strength No-Pain", "product_id": "71309-001_3371e8dc-ae55-9a65-e063-6394a90aeaac", "dosage_form": "TABLET", "product_ndc": "71309-001", "generic_name": "Acetaminophen", "labeler_name": "Safrel Pharmaceuticals, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength No-Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170731", "listing_expiration_date": "20261231"}