extra strength pain reliever

Generic: acetaminophen

Labeler: ingles markets, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength pain reliever
Generic Name acetaminophen
Labeler ingles markets, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
INGLES MARKETS, INC.

Identifiers & Regulatory

Product NDC 62936-0222
Product ID 62936-0222_115d0b60-84e9-7a34-e063-6394a90ae78c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2018-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 629360222
Hyphenated Format 62936-0222

Supplemental Identifiers

RxCUI
198440
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 pain reliever (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
  • 100 TABLET in 1 BOTTLE (62936-0222-1)
  • 50 TABLET in 1 BOTTLE (62936-0222-5)
source: ndc

Packages (2)

62936-0222-1 100 TABLET in 1 BOTTLE (62936-0222-1) 62936-0222-5 50 TABLET in 1 BOTTLE (62936-0222-5)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Extra Strength Pain Reliever ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "115d0b60-84e9-7a34-e063-6394a90ae78c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["115d0b4f-6f0f-79a9-e063-6394a90ab18a"], "manufacturer_name": ["INGLES MARKETS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62936-0222-1)", "package_ndc": "62936-0222-1", "marketing_start_date": "20190901"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (62936-0222-5)", "package_ndc": "62936-0222-5", "marketing_start_date": "20190901"}], "brand_name": "Extra Strength Pain Reliever", "product_id": "62936-0222_115d0b60-84e9-7a34-e063-6394a90ae78c", "dosage_form": "TABLET", "product_ndc": "62936-0222", "generic_name": "Acetaminophen", "labeler_name": "INGLES MARKETS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Extra Strength Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180801", "listing_expiration_date": "20261231"}