carboxymethylcellulose sodium
- Product NDC
- 50268-066
- 11-digit product format
- 502680066
- Labeler code
- 50268
- Product ID
- 50268-066_ed84f279-d01b-36cb-e053-2995a90aa66f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Carboxymethylcellulose sodium
- Dosage form
- GEL
- Route
- OPHTHALMIC
- Labeler
- AvPAK
- Application
- part349
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-11-18
- Marketing end
- 0000-00-00
- Substance
- CARBOXYMETHYLCELLULOSE SODIUM
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50268-066-15 | carboxymethylcellulose sodium | 1 in 1 CARTON | GEL | 1 | | 6 |
| 50268-066-15 | carboxymethylcellulose sodium | 15 mL in 1 BOTTLE, DROPPER | GEL | 15 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-066 | CARBOXYMETHYLCELLULOSE SODIUM GEL [AVPAK] | 6 | Legacy NDC, 2 package rows | 20240308_b469f1c4-bd94-6f50-e053-2995a90a452f.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 |
|---|
| 50268-066-15 | 50268006615 | 1 BOTTLE, DROPPER in 1 CARTON (50268-066-15) > 15 mL in 1 BOTTLE, DROPPER | 2020-11-18 | 0000-00-00 | No | No | Current |