mucinex rapid clear day night and clear and cool nasal

Generic: acetaminophen, guaifenesin, dextromethorphan hydrobromide, triprolidine hydrochloride, and oxymetazoline hydrochloride

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

Drug Facts

Product Profile

Brand Name mucinex rapid clear day night and clear and cool nasal
Generic Name acetaminophen, guaifenesin, dextromethorphan hydrobromide, triprolidine hydrochloride, and oxymetazoline hydrochloride
Labeler rb health (us) llc
Dosage Form KIT
Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-213
Product ID 72854-213_37dcb0ed-df57-1bec-e063-6394a90a695e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854213
Hyphenated Format 72854-213

Supplemental Identifiers

RxCUI
602617 1000990 2549034
UPC
0363824999517

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 rapid clear day night and clear and cool nasal (source: ndc)
Generic Name acetaminophen, guaifenesin, dextromethorphan hydrobromide, triprolidine hydrochloride, and oxymetazoline hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 200 mg
  • 10 mg
  • 1.25 mg
  • 0.05 %
source: label
Packaging
  • 1 KIT in 1 CARTON (72854-213-03) / 1 KIT in 1 KIT * 8 TABLET, COATED in 1 BLISTER PACK * 22 mL in 1 BOTTLE, PUMP * 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

72854-213-03 1 KIT in 1 CARTON (72854-213-03) / 1 KIT in 1 KIT * 8 TABLET, COATED in 1 BLISTER PACK * 22 mL in 1 BOTTLE, PUMP * 12 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

MUCINEX Rapid Clear Day Night and Clear and Cool Nasal ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "37dcb0ed-df57-1bec-e063-6394a90a695e", "openfda": {"upc": ["0363824999517"], "rxcui": ["602617", "1000990", "2549034"], "spl_set_id": ["37dcb0ed-df56-1bec-e063-6394a90a695e"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (72854-213-03)  / 1 KIT in 1 KIT *  8 TABLET, COATED in 1 BLISTER PACK *  22 mL in 1 BOTTLE, PUMP *  12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "72854-213-03", "marketing_start_date": "20250601"}], "brand_name": "MUCINEX Rapid Clear Day Night and Clear and Cool Nasal", "product_id": "72854-213_37dcb0ed-df57-1bec-e063-6394a90a695e", "dosage_form": "KIT", "product_ndc": "72854-213", "generic_name": "Acetaminophen, Guaifenesin, Dextromethorphan Hydrobromide, Triprolidine Hydrochloride, and Oxymetazoline hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCINEX Rapid Clear Day Night and Clear and Cool Nasal", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250601", "listing_expiration_date": "20261231"}