panadol

Generic: acetaminophen

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name panadol
Generic Name acetaminophen
Labeler haleon us holdings llc
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0135-0539
Product ID 0135-0539_10c14ee5-017b-0434-e063-6394a90af0f4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2012-10-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01350539
Hyphenated Format 0135-0539

Supplemental Identifiers

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 panadol (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 in 1 CARTON (0135-0539-02) / 54.7 mL in 1 BOTTLE
source: ndc

Packages (1)

0135-0539-02 1 BOTTLE in 1 CARTON (0135-0539-02) / 54.7 mL in 1 BOTTLE

Ingredients (1)

acetaminophen (160 mg/5mL)

Linked Drug Pages (1)

PANADOL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10c14ee5-017b-0434-e063-6394a90af0f4", "openfda": {"unii": ["362O9ITL9D"], "spl_set_id": ["95801755-db54-4ad7-bec1-52671914f6ca"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0135-0539-02)  / 54.7 mL in 1 BOTTLE", "package_ndc": "0135-0539-02", "marketing_start_date": "20121015"}], "brand_name": "PANADOL", "product_id": "0135-0539_10c14ee5-017b-0434-e063-6394a90af0f4", "dosage_form": "SUSPENSION", "product_ndc": "0135-0539", "generic_name": "acetaminophen", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PANADOL", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20121015", "listing_expiration_date": "20261231"}