daytime cold and flu multi-symptom relief

Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride

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

Drug Facts

Product Profile

Brand Name daytime cold and flu multi-symptom relief
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride
Labeler chain drug consortium, llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
Chain Drug Consortium, LLC

Identifiers & Regulatory

Product NDC 68016-877
Product ID 68016-877_b146c0c0-a06d-4ebf-9914-83178dde8628
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2019-07-12

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68016877
Hyphenated Format 68016-877

Supplemental Identifiers

RxCUI
1086997
UNII
362O9ITL9D 9D2RTI9KYH 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 daytime cold and flu multi-symptom relief (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 8 BLISTER PACK in 1 CARTON (68016-877-16) / 2 CAPSULE in 1 BLISTER PACK
  • 12 BLISTER PACK in 1 CARTON (68016-877-24) / 2 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (2)

68016-877-16 8 BLISTER PACK in 1 CARTON (68016-877-16) / 2 CAPSULE in 1 BLISTER PACK 68016-877-24 12 BLISTER PACK in 1 CARTON (68016-877-24) / 2 CAPSULE in 1 BLISTER PACK

Ingredients (3)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

DAYTIME COLD AND FLU MULTI-SYMPTOM RELIEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b146c0c0-a06d-4ebf-9914-83178dde8628", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["8cb0d0c8-c565-4c5a-97c5-8250a67e23a8"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 BLISTER PACK in 1 CARTON (68016-877-16)  / 2 CAPSULE in 1 BLISTER PACK", "package_ndc": "68016-877-16", "marketing_start_date": "20190712"}, {"sample": false, "description": "12 BLISTER PACK in 1 CARTON (68016-877-24)  / 2 CAPSULE in 1 BLISTER PACK", "package_ndc": "68016-877-24", "marketing_start_date": "20190712"}], "brand_name": "DAYTIME COLD AND FLU MULTI-SYMPTOM RELIEF", "product_id": "68016-877_b146c0c0-a06d-4ebf-9914-83178dde8628", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "68016-877", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DAYTIME COLD AND FLU MULTI-SYMPTOM RELIEF", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190712", "listing_expiration_date": "20261231"}