United States · FDA National Drug Code directory
Robitussin Maximum Strength Severe Multi-Symptom 7 in 1 Relief Nighttime
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
- 0031-8744_156fd078-37b4-ddce-e063-6294a90ae226
- Product NDC
- 0031-8744
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate
- Labeler
- Haleon US Holdings LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20150701
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 325 mg/1
- DEXTROMETHORPHAN HYDROBROMIDE — 15 mg/1
- DOXYLAMINE SUCCINATE — 6.25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 BLISTER PACK in 1 CARTON (0031-8744-10) / 2 CAPSULE, LIQUID FILLED in 1 BLISTER PACK · 0031-8744-10
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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