United States · FDA National Drug Code directory
Dynarex Povidone Iodine Prep Solution
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
- 67777-141_275871a0-3173-c7fa-e063-6394a90ac014
- Product NDC
- 67777-141
- Form
- LIQUID
- Composition / generic term
- Povidone Iodine Prep Solution
- Labeler
- Dynarex Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20180508
- Source listing expiry
- 20261231
Source-listed ingredients
- POVIDONE-IODINE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 48 BOTTLE in 1 CASE (67777-141-31) / 118 mL in 1 BOTTLE (67777-141-30) · 67777-141-31
- 24 BOTTLE in 1 CASE (67777-141-41) / 237 mL in 1 BOTTLE (67777-141-40) · 67777-141-41
- 24 BOTTLE in 1 CASE (67777-141-51) / 473 mL in 1 BOTTLE (67777-141-50) · 67777-141-51
- 4 BOTTLE in 1 CASE (67777-141-61) / 3790 mL in 1 BOTTLE (67777-141-60) · 67777-141-61
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →