Iodine
- Product NDC
- 41163-088
- 11-digit product format
- 411630088
- Labeler code
- 41163
- Product ID
- 41163-088_4af729f3-e20c-e7e0-e063-6294a90aca80
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Iodine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- United Natural Foods, Inc. dba UNFI
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2005-02-04
- Substance
- IODINE
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Iodine
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IODINE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9679TC07X4 |
| Rxcui | 311093 |
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 |
|---|
| 41163-088-10 | Iodine | 30 mL in 1 BOTTLE, PLASTIC | LIQUID | 30 | | 18 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41163-088 | IODINE LIQUID [UNITED NATURAL FOODS, INC. DBA UNFI] | 16 | Current NDC, Legacy NDC, 1 package rows | 20240915_8e840855-d210-4a99-b73f-6c69dcf2b6fb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41163-088-10 | 41163008810 | 30 mL in 1 BOTTLE, PLASTIC (41163-088-10) | 30 ml | 2005-02-04 | 0000-00-00 | No | No | Current |