up and up infants acetaminophen

Generic: acetaminophen

Labeler: target corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name up and up infants acetaminophen
Generic Name acetaminophen
Labeler target corporation
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

acetaminophen 160 mg/5mL

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-266
Product ID 11673-266_382b9615-d700-48aa-9d8b-35190a500c7d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2015-04-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673266
Hyphenated Format 11673-266

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 up and up infants acetaminophen (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 (11673-266-16) / 59 mL in 1 BOTTLE
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": "382b9615-d700-48aa-9d8b-35190a500c7d", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["307668"], "spl_set_id": ["31104956-04d7-41b5-82be-219ded5c02a9"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-266-16)  / 59 mL in 1 BOTTLE", "package_ndc": "11673-266-16", "marketing_start_date": "20150421"}], "brand_name": "up and up infants acetaminophen", "product_id": "11673-266_382b9615-d700-48aa-9d8b-35190a500c7d", "dosage_form": "SUSPENSION", "product_ndc": "11673-266", "generic_name": "Acetaminophen", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up infants acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "160 mg/5mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150421", "listing_expiration_date": "20261231"}