pain reliever
Generic: acetaminophen
Labeler: lidl us llcDrug Facts
Product Profile
Brand Name
pain reliever
Generic Name
acetaminophen
Labeler
lidl us llc
Dosage Form
TABLET, COATED
Routes
Active Ingredients
acetaminophen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71141-176
Product ID
71141-176_458b364a-a3ef-24ac-e063-6394a90ad1b8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2022-11-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71141176
Hyphenated Format
71141-176
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET, COATED in 1 BOTTLE, PLASTIC (71141-176-32)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "458b364a-a3ef-24ac-e063-6394a90ad1b8", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ec543339-20ab-2cba-e053-2995a90ac740"], "manufacturer_name": ["LIDL US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE, PLASTIC (71141-176-32)", "package_ndc": "71141-176-32", "marketing_start_date": "20221123"}], "brand_name": "Pain Reliever", "product_id": "71141-176_458b364a-a3ef-24ac-e063-6394a90ad1b8", "dosage_form": "TABLET, COATED", "product_ndc": "71141-176", "generic_name": "Acetaminophen", "labeler_name": "LIDL US LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221123", "listing_expiration_date": "20261231"}