Iodine
- Product NDC
- 0869-0088
- 11-digit product format
- 008690088
- Labeler code
- 0869
- Product ID
- 0869-0088_34801c77-ca7e-4a9a-9a32-cdc22428de2b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Iodine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Vi-Jon, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-08-07
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0869-0088-10 | 00869008810 | 30 mL in 1 BOTTLE, PLASTIC (0869-0088-10) | 30 ml | 2017-08-07 | 0000-00-00 | No | No | Current |