Freskaro Decolorized Iodine
- Product NDC
- 82645-207
- 11-digit product format
- 826450207
- Labeler code
- 82645
- Product ID
- 82645-207_0d99d51f-ba65-9536-e063-6394a90aecd3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pharma Nobis, LLC
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-05-16
- Substance
- ALCOHOL
- Active strength
- .48 mL/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Freskaro Decolorized Iodine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | .48 mL/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1804178 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82645-207-92 | Freskaro Decolorized Iodine | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82645-207 | FRESKARO DECOLORIZED IODINE (ALCOHOL) LIQUID [PHARMA NOBIS, LLC] | 2 | Current NDC, 1 package rows | 20231229_fbd222a2-1151-99b9-e053-6394a90a8bb8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82645-207-92 | 82645020792 | 59 mL in 1 BOTTLE, PLASTIC (82645-207-92) | 59 ml | 2023-05-16 | No | No | Current |