vicks dayquil kids cold cough plus mucus

Generic: guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide

Labeler: the procter & gamble manufacturing company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name vicks dayquil kids cold cough plus mucus
Generic Name guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide
Labeler the procter & gamble manufacturing company
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 10 mg/15mL, guaifenesin 100 mg/15mL, phenylephrine hydrochloride 5 mg/15mL

Manufacturer
The Procter & Gamble Manufacturing Company

Identifiers & Regulatory

Product NDC 69423-946
Product ID 69423-946_402e40c8-a6b9-9ac7-e063-6294a90a9dda
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-07-08

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69423946
Hyphenated Format 69423-946

Supplemental Identifiers

RxCUI
2566816
UPC
0323900042698
UNII
9D2RTI9KYH 495W7451VQ 04JA59TNSJ
NUI
N0000193956 N0000008867 N0000009560

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 vicks dayquil kids cold cough plus mucus (source: ndc)
Generic Name guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/15mL
  • 100 mg/15mL
  • 5 mg/15mL
source: ndc
Packaging
  • 236 mL in 1 BOTTLE, PLASTIC (69423-946-08)
source: ndc

Packages (1)

69423-946-08 236 mL in 1 BOTTLE, PLASTIC (69423-946-08)

Ingredients (3)

dextromethorphan hydrobromide (10 mg/15mL) guaifenesin (100 mg/15mL) phenylephrine hydrochloride (5 mg/15mL)

Linked Drug Pages (1)

Vicks DayQuil Kids Cold Cough plus Mucus ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "402e40c8-a6b9-9ac7-e063-6294a90a9dda", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0323900042698"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["2566816"], "spl_set_id": ["c6f13d96-5136-63a0-e053-2a95a90af6dc"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["The Procter & Gamble Manufacturing Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 BOTTLE, PLASTIC (69423-946-08)", "package_ndc": "69423-946-08", "marketing_start_date": "20210708"}], "brand_name": "Vicks DayQuil Kids Cold Cough plus Mucus", "product_id": "69423-946_402e40c8-a6b9-9ac7-e063-6294a90a9dda", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "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": "69423-946", "generic_name": "GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE AND DEXTROMETHORPHAN HYDROBROMIDE", "labeler_name": "The Procter & Gamble Manufacturing Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Vicks DayQuil Kids", "brand_name_suffix": "Cold Cough plus Mucus", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/15mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/15mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/15mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210708", "listing_expiration_date": "20261231"}