Eyewash
- Product NDC
- 17478-620
- 11-digit product format
- 174780620
- Labeler code
- 17478
- Product ID
- 17478-620_1d69d980-4b81-4ff9-a1ba-5d83ac0e61a2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Water
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Akorn
- Application
- NDA022305
- Marketing category
- NDA
- Marketing start
- 2014-06-01
- Marketing end
- 0000-00-00
- Substance
- WATER
- Active strength
- 929 g/946mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-620 | EYEWASH (WATER) SOLUTION [AKORN] | 6 | Legacy NDC | 20220715_bdc2d61a-b403-4263-85cb-d524cc7c6334.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-620-04 | 17478062004 | 1 BOTTLE in 1 BOTTLE (17478-620-04) > 118 mL in 1 BOTTLE | 1 bottle | 2014-06-01 | 0000-00-00 | No | No | Current |