Provodine
- Product NDC
- 59426-001
- 11-digit product format
- 594260001
- Labeler code
- 59426
- Product ID
- 59426-001_e771a266-8743-4a45-87e3-ea88acf2e9cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- providone iodine
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- Microdermis Corporation
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-09-15
- Marketing end
- 0000-00-00
- Substance
- POVIDONE-IODINE
- Active strength
- 8 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 59426-001-03 | Provodine | 3 mL in 1 PACKET | EMULSION | 3 | | 4 |
| 59426-001-03 | Provodine | 100 in 1 BOX | EMULSION | 100 | | 4 |
| 59426-001-04 | Provodine | 118 mL in 1 BOTTLE | EMULSION | 118 | | 4 |
| 59426-001-16 | Provodine | 473 mL in 1 BOTTLE | EMULSION | 473 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59426-001 | PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION] | 4 | Legacy NDC, 4 package rows | 20150703_6819df87-aaf8-49f8-a95d-acb6926d6848.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 59426-001-03 | 59426000103 | 3 mL in 1 PACKET | 3 ml | Historical |
| 59426-001-04 | 59426000104 | 118 mL in 1 BOTTLE | 118 ml | Historical |
| 59426-001-16 | 59426000116 | 473 mL in 1 BOTTLE | 473 ml | Historical |