Dry Eye Relief
- Product NDC
- 70000-0089
- 11-digit product format
- 700000089
- Labeler code
- 70000
- Product ID
- 70000-0089_b2fd3f1c-69bb-4c0c-9a11-1c135377045c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carboxymethylcellulose sodium
- Dosage form
- GEL
- Route
- OPHTHALMIC
- Labeler
- CARDINAL HEALTH 110, LLC. DBA LEADER
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-03-09
- Marketing end
- 2026-11-30
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dry Eye Relief
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | K679OBS311 |
| Rxcui | 579907 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70000-0089-1 | Dry Eye Relief | 1 in 1 CARTON | GEL | 1 | | 3 |
| 70000-0089-1 | Dry Eye Relief | 15 mL in 1 BOTTLE, DROPPER | GEL | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70000-0089 | DRY EYE RELIEF (CARBOXYMETHYLCELLULOSE SODIUM) GEL [CARDINAL HEALTH, 110 DBA LEADER] | 2 | Current NDC, Legacy NDC, 2 package rows | 20210701_bd262028-32e9-052d-e053-2a95a90a5303.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70000-0089-1 | 70000008901 | 1 BOTTLE, DROPPER in 1 CARTON (70000-0089-1) / 15 mL in 1 BOTTLE, DROPPER | 2021-03-09 | 2026-11-30 | No | No | Current |