Major Lubricating Eye Drops
- Product NDC
- 0904-6848
- 11-digit product format
- 009046848
- Labeler code
- 0904
- Product ID
- 0904-6848_a97ff9b6-e406-089a-e053-2995a90acc99
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carboxymethylcellulose Sodium
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Harvard Drug Group L L C
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-06-23
- Marketing end
- 0000-00-00
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
- Active strength
- 1 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 0904-6848 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 0904-6848 | 0904-6848-46 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 0904-6848 | 0904-6848-51 | D | Discontinued by firm | 2026-10-05 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 0904-6848-46 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 0904-6848-51 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 0904-6848-46 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 0904-6848-51 | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 0904-6848-46 | 00904684846 | 30 VIAL, SINGLE-USE in 1 BOX (0904-6848-46) > .4 mL in 1 VIAL, SINGLE-USE | 2020-06-23 | 0000-00-00 | No | No | Current |
| 0904-6848-51 | 00904684851 | 50 VIAL, SINGLE-USE in 1 BOX (0904-6848-51) > .4 mL in 1 VIAL, SINGLE-USE | 2020-06-23 | 0000-00-00 | No | No | Current |