Iodine
- Product NDC
- 50804-088
- 11-digit product format
- 508040088
- Labeler code
- 50804
- Product ID
- 50804-088_51d752c5-0390-4a5f-872f-70a32bbff593
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Iodine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Perrigo Direct, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2008-11-08
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL; IODINE; SODIUM IODIDE
- Active strength
- 470 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50804-088 | IODINE LIQUID [PERRIGO DIRECT, INC.] | 10 | Legacy NDC | 20240920_3b424440-5bb7-4207-9884-1461a54fbe0b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-088-10 | 50804008810 | 30 mL in 1 BOTTLE, PLASTIC (50804-088-10) | 30 ml | 2008-11-08 | 0000-00-00 | No | No | Current |