Nighttime Relief Lubricant
- Product NDC
- 46122-757
- 11-digit product format
- 461220757
- Labeler code
- 46122
- Product ID
- 46122-757_473537d8-7caa-2415-e063-6294a90afc68
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Light Mineral Oil, White Petrolatum
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Amerisource Bergen Drug Corp.
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-06-05
- Substance
- LIGHT MINERAL OIL; WHITE PETROLATUM
- Active strength
- 425; 573 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nighttime Relief Lubricant
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIGHT MINERAL OIL | 425 mg/g |
| WHITE PETROLATUM | 573 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N6K5787QVP, B6E5W8RQJ4 |
| Rxcui | 702008 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 46122-757-37 | Nighttime Relief Lubricant | 1 in 1 BOX | OINTMENT | 1 | | 3 |
| 46122-757-37 | Nighttime Relief Lubricant | 3.5 g in 1 TUBE | OINTMENT | 3.5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 46122-757 | NIGHTTIME RELIEF LUBRICANT (LIGHT MINERAL OIL, WHITE PETROLATUM) OINTMENT [AMERISOURCE BERGEN DRUG CORP.] | 2 | Current NDC, 2 package rows | 20231224_fd6b2be8-7e00-3765-e053-6294a90a4061.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 46122-757-37 | 46122075737 | 1 TUBE in 1 BOX (46122-757-37) / 3.5 g in 1 TUBE | 1 tube | 2023-06-05 | No | No | Historical |