Retaine Ultra PF
NDC 54799-470, Polyethylene Glycol, liquid, from OCuSOFT LLC.
- Product NDC
- 54799-470
- Status
- Listed
- Labeler
- OCuSOFT LLC
- Dosage form
- LIQUID
- Route
- OPHTHALMIC
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M018
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/54799-470 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- POLYETHYLENE GLYCOL 4004 mg/mL
- PROPYLENE GLYCOL3 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 54799-470-10 | 54799047010 | 10 mL in 1 BOTTLE, DROPPER (54799-470-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 54799-470 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/54799-470 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 54799-470. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.