United States · FDA National Drug Code directory

Mucinex Fast-Max Day Cold and Flu and Mucinex Nightshift Night Severe Cold and Flu Maximum Strength

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
72854-169_522dc3c2-13c5-efaa-e063-6394a90ae25d
Product NDC
72854-169
Form
KIT
Composition / generic term
acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride
Labeler
Reckitt Benckiser LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20250701
Source listing expiry
20271231

Source-listed ingredients

Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 KIT in 1 CARTON (72854-169-10) / 1 KIT in 1 KIT * 6 TABLET in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK · 72854-169-10
  • 2 KIT in 1 CARTON (72854-169-20) / 1 KIT in 1 KIT * 6 TABLET in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK · 72854-169-20
  • 4 KIT in 1 CARTON (72854-169-40) / 1 KIT in 1 KIT * 6 TABLET in 1 BLISTER PACK * 4 TABLET, COATED in 1 BLISTER PACK · 72854-169-40

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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