De La Cruz Decolorized Iodine
- Product NDC
- 24286-1529
- 11-digit product format
- 242861529
- Labeler code
- 24286
- Product ID
- 24286-1529_299414ed-41eb-0dbb-e063-6394a90a88f9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- DLC Laboratories, Inc.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1998-03-25
- Substance
- ALCOHOL
- Active strength
- .45 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
- De La Cruz Decolorized Iodine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | .45 mL/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24286-1529-8 | De La Cruz Decolorized Iodine | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24286-1529 | DE LA CRUZ DECOLORIZED IODINE (ETHYL ALCOHOL) LIQUID [DLC LABORATORIES, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241220_5d8f6aaa-0b87-1166-e053-2991aa0a297f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24286-1529-8 | 24286152908 | 59 mL in 1 BOTTLE, PLASTIC (24286-1529-8) | 59 ml | 2017-11-06 | 0000-00-00 | No | No | Current |