IODDO
- Product NDC
- 84178-005
- 11-digit product format
- 841780005
- Labeler code
- 84178
- Product ID
- 84178-005_4af8552c-1f2c-84ad-e063-6394a90abb62
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- IODINE
- Dosage form
- TINCTURE
- Route
- TOPICAL
- Labeler
- EVI LABS
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-09
- Substance
- IODINE
- Active strength
- .56 g/28g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- IODDO
- Brand name suffix
- IODINE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IODINE | .56 g/28g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9679TC07X4 |
| Rxcui | 311093 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84178-005-03 | IODDOIODINE | 28 g in 1 BOTTLE, PLASTIC | TINCTURE | 28 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84178-005-03 | 84178000503 | 28 g in 1 BOTTLE, PLASTIC (84178-005-03) | 28 g | 2026-03-09 | No | No | Historical |