United States · FDA National Drug Code directory
Dynarex Green
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
- 67777-308_2758dc6f-a18e-fc43-e063-6294a90aade6
- Product NDC
- 67777-308
- Form
- LIQUID
- Composition / generic term
- ALCOHOL
- Labeler
- Dynarex Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20140701
- Source listing expiry
- 20261231
Source-listed ingredients
- ALCOHOL — .3 mL/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 59 mL in 1 BOTTLE (67777-308-03) · 67777-308-03
- 12 BOTTLE in 1 CASE (67777-308-11) / 473 mL in 1 BOTTLE (67777-308-01) · 67777-308-11
- 4 BOTTLE in 1 CASE (67777-308-12) / 3785 mL in 1 BOTTLE (67777-308-02) · 67777-308-12
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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