Humco Strong Iodine
- Product NDC
- 0395-2775
- 11-digit product format
- 003952775
- Labeler code
- 0395
- Product ID
- 0395-2775_da6c5009-ea01-25c6-e053-2995a90ab727
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Iodine and potassium iodide
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Humco Holding Group, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2008-01-01
- Marketing end
- 0000-00-00
- Substance
- IODINE; POTASSIUM IODIDE
- Active strength
- 50 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Additional Listing Data#
- Finished product
- No
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IODINE | 50 mg/mL |
| POTASSIUM IODIDE | 100 mg/mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0395-2775-16 | 00395277516 | 473 mL in 1 BOTTLE, PLASTIC (0395-2775-16) | 473 ml | 2017-11-14 | 0000-00-00 | No | No | Current |