up and up nighttime flu and severe cold and cough

Generic: acetaminophen, diphenhydramine hydrochloride, and phenylephrine hydrochloride

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

Drug Facts

Product Profile

Brand Name up and up nighttime flu and severe cold and cough
Generic Name acetaminophen, diphenhydramine hydrochloride, and phenylephrine hydrochloride
Labeler target corporation
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1, diphenhydramine hydrochloride 25 mg/1, phenylephrine hydrochloride 10 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-113
Product ID 11673-113_39fadcca-6c94-39b8-e063-6394a90a89a2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2013-06-28

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673113
Hyphenated Format 11673-113

Supplemental Identifiers

RxCUI
1659960
UNII
362O9ITL9D TC2D6JAD40 04JA59TNSJ

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 nighttime flu and severe cold and cough (source: ndc)
Generic Name acetaminophen, diphenhydramine hydrochloride, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
  • 25 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 6 POWDER, FOR SOLUTION in 1 CARTON (11673-113-07)
source: ndc

Packages (1)

11673-113-07 6 POWDER, FOR SOLUTION in 1 CARTON (11673-113-07)

Ingredients (3)

acetaminophen (650 mg/1) diphenhydramine hydrochloride (25 mg/1) phenylephrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

up and up nighttime flu and severe cold and cough ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39fadcca-6c94-39b8-e063-6394a90a89a2", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1659960"], "spl_set_id": ["df488727-b913-440b-9a0b-cce3ae143bf2"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER, FOR SOLUTION in 1 CARTON (11673-113-07)", "package_ndc": "11673-113-07", "marketing_start_date": "20130628"}], "brand_name": "up and up nighttime flu and severe cold and cough", "product_id": "11673-113_39fadcca-6c94-39b8-e063-6394a90a89a2", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "11673-113", "generic_name": "Acetaminophen, Diphenhydramine hydrochloride, and Phenylephrine hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up", "brand_name_suffix": "nighttime flu and severe cold and cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130628", "listing_expiration_date": "20261231"}