Carboxymethylcellulose Sodium Eye Drops 0.5%
- Product NDC
- 16030-501
- 11-digit product format
- 160300501
- Labeler code
- 16030
- Product ID
- 16030-501_495c072a-fa45-45a7-e063-6394a90ad7d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carboxymethylcellulose Sodium Eye Drops 0.5%
- Dosage form
- FOR SOLUTION
- Route
- TOPICAL
- Labeler
- Aurolab
- Application
- M018
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-09-20
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
- 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
- Carboxymethylcellulose Sodium Eye Drops 0.5%
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED | 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 |
|---|
| 16030-501-05 | Carboxymethylcellulose Sodium Eye Drops 0.5% | 5 mL in 1 BOTTLE, DROPPER | FOR SOLUTION | 5 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16030-501 | CARBOXYMETHYLCELLULOSE SODIUM EYE DROPS 0.5% FOR SOLUTION [AUROLAB] | 8 | Current NDC, Legacy NDC, 1 package rows | 20250413_e8b4df3b-3d81-b3ca-e053-2a95a90af2ec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16030-501-05 | 16030050105 | 5 mL in 1 BOTTLE, DROPPER (16030-501-05) | 5 ml | 2022-09-20 | 0000-00-00 | No | No | Current |