pain reliever extra strength

Generic: acetaminophen

Labeler: walgreens
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain reliever extra strength
Generic Name acetaminophen
Labeler walgreens
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/15mL

Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-0278
Product ID 0363-0278_9596606a-d83c-44a9-9cbf-89b27ed87e30
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2016-01-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630278
Hyphenated Format 0363-0278

Supplemental Identifiers

RxCUI
307684
UPC
0311917157993
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 reliever extra strength (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/15mL
source: ndc
Packaging
  • 237 mL in 1 BOTTLE, PLASTIC (0363-0278-08)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (500 mg/15mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9596606a-d83c-44a9-9cbf-89b27ed87e30", "openfda": {"upc": ["0311917157993"], "unii": ["362O9ITL9D"], "rxcui": ["307684"], "spl_set_id": ["b4b06d32-6a09-4c43-980b-377b617ba739"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (0363-0278-08)", "package_ndc": "0363-0278-08", "marketing_start_date": "20160131"}], "brand_name": "Pain Reliever Extra Strength", "product_id": "0363-0278_9596606a-d83c-44a9-9cbf-89b27ed87e30", "dosage_form": "LIQUID", "product_ndc": "0363-0278", "generic_name": "Acetaminophen", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160131", "listing_expiration_date": "20261231"}