De La Cruz Tincture of Iodine
- Product NDC
- 24286-1528
- 11-digit product format
- 242861528
- Labeler code
- 24286
- Product ID
- 24286-1528_0c940d4f-cca2-7175-e063-6394a90af568
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Iodine and Sodium Iodide and Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- DLC Laboratories, Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1979-01-01
- Substance
- ALCOHOL; IODINE; SODIUM IODIDE
- Active strength
- 470; 20; 20.4 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- De La Cruz Tincture of Iodine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 470 mg/mL |
| IODINE | 20 mg/mL |
| SODIUM IODIDE | 20.4 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M, 9679TC07X4, F5WR8N145C |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24286-1528-7 | De La Cruz Tincture of Iodine | 30 mL in 1 BOTTLE | LIQUID | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24286-1528 | DE LA CRUZ TINCTURE OF IODINE (IODINE AND SODIUM IODIDE AND ALCOHOL) LIQUID [DLC LABORATORIES, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20231216_5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24286-1528-7 | 24286152807 | 30 mL in 1 BOTTLE (24286-1528-7) | 30 ml | 2017-10-27 | 0000-00-00 | No | No | Current |