United States · FDA National Drug Code directory
Retaine Ultra PF
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
- 54799-470_73f4c537-3cc4-49cd-a580-9adfb7e5f4fb
- Product NDC
- 54799-470
- Form
- LIQUID
- Composition / generic term
- Polyethylene Glycol
- Labeler
- OCuSOFT LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20260519
- Source listing expiry
- 20271231
Source-listed ingredients
- POLYETHYLENE GLYCOL 400 — 4 mg/mL
- PROPYLENE GLYCOL — 3 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 mL in 1 BOTTLE, DROPPER (54799-470-10) · 54799-470-10
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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