United States · FDA National Drug Code directory
Tukol Max Action
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
- 50066-518_d2a614d3-f9b2-4da8-8c7e-a0993d55cd90
- Product NDC
- 50066-518
- Form
- LIQUID
- Composition / generic term
- oxymetazoline hydrochloride
- Labeler
- Genomma Lab USA
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250212
- Source listing expiry
- 20261231
Source-listed ingredients
- OXYMETAZOLINE HYDROCHLORIDE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, SPRAY in 1 CARTON (50066-518-05) / 15 mL in 1 BOTTLE, SPRAY · 50066-518-05
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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