dye free pain reliever childrens

Generic: acetaminophen

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dye free pain reliever childrens
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 49580-0685
Product ID 49580-0685_f446b9fa-069b-48e1-8ae4-ec5ad945f67c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2018-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 495800685
Hyphenated Format 49580-0685

Supplemental Identifiers

RxCUI
307668
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 dye free pain reliever childrens (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 (49580-0685-4) / 118 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f446b9fa-069b-48e1-8ae4-ec5ad945f67c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["45ddcaad-d416-4d7c-a84a-43548d5c5d3b"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 BOX (49580-0685-4)  / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "49580-0685-4", "marketing_start_date": "20180228"}], "brand_name": "Dye Free Pain Reliever Childrens", "product_id": "49580-0685_f446b9fa-069b-48e1-8ae4-ec5ad945f67c", "dosage_form": "SUSPENSION", "product_ndc": "49580-0685", "generic_name": "Acetaminophen", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dye Free Pain Reliever", "brand_name_suffix": "Childrens", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180228", "listing_expiration_date": "20261231"}