Walgreens Ultra Lubricant
- Product NDC
- 0363-6154
- 11-digit product format
- 003636154
- Labeler code
- 0363
- Product ID
- 0363-6154_41605179-6e0c-9252-e063-6394a90afaeb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Polyethylene Glycol 400, and Propylene Glycol
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Walgreens
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-29
- Substance
- POLYETHYLENE GLYCOL 400; PROPYLENE GLYCOL
- Active strength
- 4; 3 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Walgreens Ultra Lubricant
- Listing expiration
- 2026-12-31
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 |
|---|
| 0363-6154-05 | Walgreens Ultra Lubricant | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | | 3 |
| 0363-6154-05 | Walgreens Ultra Lubricant | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-6154-05 | 00363615405 | 1 BOTTLE, DROPPER in 1 CARTON (0363-6154-05) / 15 mL in 1 BOTTLE, DROPPER | 2025-08-29 | No | No | Historical |