Retaine Ultra PF
- Product NDC
- 54799-470
- 11-digit product format
- 547990470
- Labeler code
- 54799
- Product ID
- 54799-470_73f4c537-3cc4-49cd-a580-9adfb7e5f4fb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Polyethylene Glycol
- Dosage form
- LIQUID
- Route
- OPHTHALMIC
- Labeler
- OCuSOFT LLC
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-19
- Substance
- POLYETHYLENE GLYCOL 400; PROPYLENE GLYCOL
- Active strength
- 4; 3 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Retaine Ultra PF
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POLYETHYLENE GLYCOL 400 | 4 mg/mL |
| PROPYLENE GLYCOL | 3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | B697894SGQ, 6DC9Q167V3 |
| Rxcui | 477589 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54799-470-10 | Retaine Ultra PF | 10 mL in 1 BOTTLE, DROPPER | LIQUID | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 54799-470-10 | 54799047010 | 10 mL in 1 BOTTLE, DROPPER (54799-470-10) | 10 ml | 2026-05-19 | No | No | Historical |