Lubricant Eye Drops
- Product NDC
- 55651-510
- 11-digit product format
- 556510510
- Labeler code
- 55651
- Product ID
- 55651-510_4bafa893-cf6c-9e19-e063-6294a90a4f7e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CARBOXYMETHYLCELLULOSE SODIUM
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- KC Pharmaceuticals, Inc.
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-25
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM
- Active strength
- 5 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
- Lubricant Eye Drops
- Listing expiration
- 2027-12-31
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 |
|---|
| 55651-510-01 | Lubricant Eye Drops | 5 in 1 BOX | SOLUTION/ DROPS | 5 | | 1 |
| 55651-510-01 | Lubricant Eye Drops | 0.4 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 0.4 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 55651-510-01 | 55651051001 | 5 BOTTLE, DROPPER in 1 BOX (55651-510-01) / .4 mL in 1 BOTTLE, DROPPER | 2026-02-25 | No | No | Historical |