maximum strength nighttime cold and flu

Generic: acetaminophen , diphenhydramine hcl,phenylephrine hcl

Labeler: the kroger co
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength nighttime cold and flu
Generic Name acetaminophen , diphenhydramine hcl,phenylephrine hcl
Labeler the kroger co
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/20mL, diphenhydramine hydrochloride 25 mg/20mL, phenylephrine hydrochloride 10 mg/20mL

Manufacturer
THE KROGER CO

Identifiers & Regulatory

Product NDC 30142-736
Product ID 30142-736_3c28fa93-4a04-9245-e063-6394a90a6871
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-09-04

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 30142736
Hyphenated Format 30142-736

Supplemental Identifiers

RxCUI
1375932
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 maximum strength nighttime cold and flu (source: ndc)
Generic Name acetaminophen , diphenhydramine hcl,phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/20mL
  • 25 mg/20mL
  • 10 mg/20mL
source: ndc
Packaging
  • 180 mL in 1 BOTTLE (30142-736-06)
source: ndc

Packages (1)

30142-736-06 180 mL in 1 BOTTLE (30142-736-06)

Ingredients (3)

acetaminophen (650 mg/20mL) diphenhydramine hydrochloride (25 mg/20mL) phenylephrine hydrochloride (10 mg/20mL)

Linked Drug Pages (1)

Maximum Strength Nighttime Cold and Flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c28fa93-4a04-9245-e063-6394a90a6871", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1375932"], "spl_set_id": ["058b2021-8a61-40b0-8a2e-a784d2b847fb"], "manufacturer_name": ["THE KROGER CO"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 mL in 1 BOTTLE (30142-736-06)", "package_ndc": "30142-736-06", "marketing_start_date": "20200904"}], "brand_name": "Maximum Strength Nighttime Cold and Flu", "product_id": "30142-736_3c28fa93-4a04-9245-e063-6394a90a6871", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "30142-736", "generic_name": "Acetaminophen , Diphenhydramine HCl,Phenylephrine HCl", "labeler_name": "THE KROGER CO", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Nighttime Cold and Flu", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/20mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200904", "listing_expiration_date": "20261231"}