mucinex childrens day time multi-symptom cold and mucinex childrens night time multi-symptom cold triple pack

Generic: acetaminophen, diphenylhydramine hydrochloride, phenylephrine hydrochloride, dextromethorphan hydrobromide, and guaifenesin

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

Drug Facts

Product Profile

Brand Name mucinex childrens day time multi-symptom cold and mucinex childrens night time multi-symptom cold triple pack
Generic Name acetaminophen, diphenylhydramine hydrochloride, phenylephrine hydrochloride, dextromethorphan hydrobromide, and guaifenesin
Labeler rb health (us) llc
Dosage Form KIT
Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 63824-944
Product ID 63824-944_29a688b2-f69d-b455-e063-6294a90a1352
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-05-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63824944
Hyphenated Format 63824-944

Supplemental Identifiers

RxCUI
1043543 1375932 2637728
UPC
0363824018416

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 day time multi-symptom cold and mucinex childrens night time multi-symptom cold triple pack (source: ndc)
Generic Name acetaminophen, diphenylhydramine hydrochloride, phenylephrine hydrochloride, dextromethorphan hydrobromide, and guaifenesin (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 10 ml
  • 325 mg
  • 12.5 mg
  • 5 mg
  • 5 ml
  • 100 mg
  • 2.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (63824-944-34) * 1 BOTTLE in 1 CARTON (63824-949-01) / 118 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (63824-950-21) / 118 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "29a688b2-f69d-b455-e063-6294a90a1352", "openfda": {"upc": ["0363824018416"], "rxcui": ["1043543", "1375932", "2637728"], "spl_set_id": ["c7ab5201-8550-4bf4-957c-c8f049aeaa4a"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (63824-944-34)  *  1 BOTTLE in 1 CARTON (63824-949-01)  / 118 mL in 1 BOTTLE *  1 BOTTLE in 1 CARTON (63824-950-21)  / 118 mL in 1 BOTTLE", "package_ndc": "63824-944-34", "marketing_start_date": "20220525"}], "brand_name": "Mucinex Childrens Day Time Multi-Symptom Cold and Mucinex Childrens Night Time Multi-Symptom Cold Triple Pack", "product_id": "63824-944_29a688b2-f69d-b455-e063-6294a90a1352", "dosage_form": "KIT", "product_ndc": "63824-944", "generic_name": "Acetaminophen, Diphenylhydramine Hydrochloride, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, and Guaifenesin", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Childrens Day Time Multi-Symptom Cold and Mucinex Childrens Night Time Multi-Symptom Cold Triple Pack", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}