pain relief

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
Generic Name acetaminophen
Labeler p & l development, llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 49580-0821
Product ID 49580-0821_fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2024-07-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 495800821
Hyphenated Format 49580-0821

Supplemental Identifiers

RxCUI
307668
UPC
0349580281059
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 (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 BOX (49580-0821-4) / 118 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

49580-0821-4 1 BOTTLE, PLASTIC in 1 BOX (49580-0821-4) / 118 mL in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5", "openfda": {"upc": ["0349580281059"], "unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["1c081a7c-8cff-4253-97ac-5fa74a5c0668"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (49580-0821-4)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "49580-0821-4", "marketing_start_date": "20240731"}], "brand_name": "Pain Relief", "product_id": "49580-0821_fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5", "dosage_form": "SUSPENSION", "product_ndc": "49580-0821", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240731", "listing_expiration_date": "20261231"}