night time severe cold and cough relief

Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl

Labeler: chain drug consortium, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name night time severe cold and cough relief
Generic Name acetaminophen, diphenhydramine hcl, phenylephrine hcl
Labeler chain drug consortium, llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/15mL, diphenhydramine hydrochloride 12.5 mg/15mL, phenylephrine hydrochloride 5 mg/15mL

Manufacturer
Chain Drug Consortium, LLC

Identifiers & Regulatory

Product NDC 68016-154
Product ID 68016-154_2f8462e8-7096-4688-ba3d-14caae022944
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2013-10-04

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 68016154
Hyphenated Format 68016-154

Supplemental Identifiers

RxCUI
1298348
UPC
0840986022845
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 night time severe cold and cough relief (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl, phenylephrine hcl (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/15mL
  • 12.5 mg/15mL
  • 5 mg/15mL
source: ndc
Packaging
  • 245 mL in 1 BOTTLE (68016-154-08)
source: ndc

Packages (1)

68016-154-08 245 mL in 1 BOTTLE (68016-154-08)

Ingredients (3)

acetaminophen (325 mg/15mL) diphenhydramine hydrochloride (12.5 mg/15mL) phenylephrine hydrochloride (5 mg/15mL)

Linked Drug Pages (1)

Night Time Severe Cold and Cough Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f8462e8-7096-4688-ba3d-14caae022944", "openfda": {"upc": ["0840986022845"], "unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1298348"], "spl_set_id": ["c8e9b57b-83e9-46c5-9791-02c4c2b94004"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "245 mL in 1 BOTTLE (68016-154-08)", "package_ndc": "68016-154-08", "marketing_start_date": "20131004"}], "brand_name": "Night Time Severe Cold and Cough Relief", "product_id": "68016-154_2f8462e8-7096-4688-ba3d-14caae022944", "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": "68016-154", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Night Time Severe Cold and Cough Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/15mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/15mL"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20131004", "listing_expiration_date": "20261231"}