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

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

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 night time multi-symptom cold
Generic Name dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, acetaminophen, and diphenhydramine hydrochloride
Labeler rb health (us) llc
Dosage Form KIT
Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 63824-955
Product ID 63824-955_29a654df-016e-830e-e063-6394a90a1062
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2019-01-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63824955
Hyphenated Format 63824-955

Supplemental Identifiers

RxCUI
1043543 1375932 2637728
UPC
0363824909943

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 night time multi-symptom cold (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, acetaminophen, and diphenhydramine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 5 ml
  • 5 mg
  • 100 mg
  • 2.5 mg
  • 10 ml
  • 325 mg
  • 12.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (63824-955-74) * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE
source: ndc

Packages (1)

63824-955-74 1 KIT in 1 CARTON (63824-955-74) * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Mucinex Childrens Day Time Multi-Symptom Cold and Night Time Multi-Symptom Cold ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "29a654df-016e-830e-e063-6394a90a1062", "openfda": {"upc": ["0363824909943"], "rxcui": ["1043543", "1375932", "2637728"], "spl_set_id": ["e3aea6df-37a4-43c5-a192-a902cbff3f92"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (63824-955-74)  *  118 mL in 1 BOTTLE *  118 mL in 1 BOTTLE", "package_ndc": "63824-955-74", "marketing_start_date": "20190121"}], "brand_name": "Mucinex Childrens Day Time Multi-Symptom Cold and Night Time Multi-Symptom Cold", "product_id": "63824-955_29a654df-016e-830e-e063-6394a90a1062", "dosage_form": "KIT", "product_ndc": "63824-955", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, Acetaminophen, and Diphenhydramine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Childrens", "brand_name_suffix": "Day Time Multi-Symptom Cold and Night Time Multi-Symptom Cold", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190121", "listing_expiration_date": "20261231"}