Refresh Tears Lubricant
- Product NDC
- 67751-130
- 11-digit product format
- 677510130
- Labeler code
- 67751
- Product ID
- 67751-130_97de3ba6-f8ec-0e2e-e053-2995a90a663c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CARBOXYMETHYLCELLULOSE SODIUM
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Navajo Manufacturing Company Inc.
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2004-09-01
- Marketing end
- 0000-00-00
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM
- Active strength
- 5 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
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 |
|---|
| 67751-130-01 | Refresh Tears Lubricant | 3 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 3 | | 14 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67751-130 | REFRESH TEARS LUBRICANT (CARBOXYMETHYLCELLULOSE SODIUM) SOLUTION/ DROPS [NAVAJO MANUFACTURING COMPANY INC.] | 14 | Legacy NDC, 1 package rows | 20241004_3b94f67c-d675-4e16-846a-3ca39b0405e0.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 |
|---|
| 67751-130-01 | 67751013001 | 3 mL in 1 BOTTLE, DROPPER (67751-130-01) | 3 ml | 2017-12-22 | 0000-00-00 | No | No | Current |