Up and Up Dry Eye Relief Lubricant Eye Drops
- Product NDC
- 11716-0771
- 11-digit product format
- 117160771
- Labeler code
- 11716
- Product ID
- 11716-0771_420274c6-7bf1-0920-e063-6294a90a30be
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carboxymethylcellulose Sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Hanlim
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-31
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM
- Active strength
- 5 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
- Up and Up Dry Eye Relief Lubricant Eye Drops
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBOXYMETHYLCELLULOSE SODIUM | 5 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K679OBS311 |
| Rxcui | 1188426 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11716-0771-1 | Up and Up Dry Eye Relief Lubricant Eye Drops | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | | 1 |
| 11716-0771-1 | Up and Up Dry Eye Relief Lubricant Eye Drops | 2 in 1 BOX | SOLUTION/ DROPS | 2 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 11716-0771-1 | 11716077101 | 2 BOTTLE, DROPPER in 1 BOX (11716-0771-1) / 15 mL in 1 BOTTLE, DROPPER | 2025-10-31 | No | No | Historical |