mucinex sinus-max day pressure, pain and cough and mucinex nightshift night sinus maximum strength
Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, triprolidine hydrochloride
Labeler: rb health (us) llcDrug Facts
Product Profile
Brand Name
mucinex sinus-max day pressure, pain and cough and mucinex nightshift night sinus maximum strength
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, triprolidine hydrochloride
Labeler
rb health (us) llc
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
72854-243
Product ID
72854-243_29f6d33e-1625-32df-e063-6294a90a9355
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2021-07-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72854243
Hyphenated Format
72854-243
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
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 sinus-max day pressure, pain and cough and mucinex nightshift night sinus maximum strength (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, triprolidine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Resolved Composition
Strengths
- 325 mg
- 10 mg
- 200 mg
- 5 mg
- 1.25 mg
Packaging
- 1 KIT in 1 CARTON (72854-243-10) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
- 2 KIT in 1 CARTON (72854-243-20) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
- 4 KIT in 1 CARTON (72854-243-40) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
Packages (3)
72854-243-10
1 KIT in 1 CARTON (72854-243-10) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
72854-243-20
2 KIT in 1 CARTON (72854-243-20) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
72854-243-40
4 KIT in 1 CARTON (72854-243-40) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "29f6d33e-1625-32df-e063-6294a90a9355", "openfda": {"rxcui": ["1110988", "2549037", "2560237"], "spl_set_id": ["c746953f-4b7d-4e2a-9b85-96bd6901f517"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72854-243-10) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-243-10", "marketing_start_date": "20210701"}, {"sample": false, "description": "2 KIT in 1 CARTON (72854-243-20) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-243-20", "marketing_start_date": "20210701"}, {"sample": false, "description": "4 KIT in 1 CARTON (72854-243-40) / 1 KIT in 1 KIT * 6 TABLET, FILM COATED in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-243-40", "marketing_start_date": "20210701"}], "brand_name": "Mucinex Sinus-Max Day Pressure, Pain and Cough and Mucinex Nightshift Night Sinus Maximum Strength", "product_id": "72854-243_29f6d33e-1625-32df-e063-6294a90a9355", "dosage_form": "KIT", "product_ndc": "72854-243", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Sinus-Max Day Pressure, Pain and Cough and Mucinex Nightshift Night Sinus", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}