United States · FDA National Drug Code directory
ACTIDOM DMX
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
- 63102-110_07838a85-4ddc-470d-a344-001587f2d904
- Product NDC
- 63102-110
- Form
- SOLUTION
- Composition / generic term
- DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
- Labeler
- ACTIPHARMA, LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20150813
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXTROMETHORPHAN HYDROBROMIDE — 30 mg/5mL
- GUAIFENESIN — 200 mg/5mL
- PHENYLEPHRINE HYDROCHLORIDE — 10 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 474 mL in 1 BOTTLE, PLASTIC (63102-110-16) · 63102-110-16
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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