mucinex childrens night time multi-symptom cold

Generic: acetaminophen, diphenhydramine hydrochloride, and phenylephrine hydrochloride

Labeler: rb health (us) llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucinex childrens night time multi-symptom cold
Generic Name acetaminophen, diphenhydramine hydrochloride, and phenylephrine hydrochloride
Labeler rb health (us) llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/10mL, diphenhydramine hydrochloride 12.5 mg/10mL, phenylephrine hydrochloride 5 mg/10mL

Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 63824-950
Product ID 63824-950_29a659fd-d4ce-2521-e063-6294a90a59f4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-05-01

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 63824950
Hyphenated Format 63824-950

Supplemental Identifiers

RxCUI
1375932
UPC
0363824600642
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 mucinex childrens night time multi-symptom cold (source: ndc)
Generic Name acetaminophen, diphenhydramine hydrochloride, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/10mL
  • 12.5 mg/10mL
  • 5 mg/10mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (63824-950-21) / 118 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (3)

acetaminophen (325 mg/10mL) diphenhydramine hydrochloride (12.5 mg/10mL) phenylephrine hydrochloride (5 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "29a659fd-d4ce-2521-e063-6294a90a59f4", "openfda": {"upc": ["0363824600642"], "unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1375932"], "spl_set_id": ["e048cd53-a3cd-484f-a972-4cb49791dba3"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63824-950-21)  / 118 mL in 1 BOTTLE", "package_ndc": "63824-950-21", "marketing_start_date": "20180501"}], "brand_name": "Mucinex Childrens Night Time Multi-Symptom Cold", "product_id": "63824-950_29a659fd-d4ce-2521-e063-6294a90a59f4", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "63824-950", "generic_name": "ACETAMINOPHEN, Diphenhydramine Hydrochloride, and Phenylephrine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Childrens", "brand_name_suffix": "Night Time Multi-Symptom Cold", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/10mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/10mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/10mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180501", "listing_expiration_date": "20261231"}