lumicain
- Product NDC
- 10733-412
- 11-digit product format
- 107330412
- Labeler code
- 10733
- Product ID
- 10733-412_b725dd26-c793-51a4-e053-2a95a90a573d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Aluminium Chloride Hexahydrate
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Medical Products Laboratories, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2010-09-29
- Substance
- ALUMINUM CHLORIDE
- Active strength
- 250 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- lumicain
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLORIDE | 250 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3CYT62D3GA |
| Rxcui | 244613, 486109 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10733-412-60 | lumicain | 67 g in 1 BOTTLE | SOLUTION | 67 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10733-412 | LUMICAIN (ALUMINIUM CHLORIDE HEXAHYDRATE) SOLUTION [MEDICAL PRODUCTS LABORATORIES, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20201224_9fdcce3e-e4d4-41ae-8609-37987c12414e.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 |
|---|
| 10733-412-60 | 10733041260 | 67 g in 1 BOTTLE (10733-412-60) | 67 g | 2020-09-29 | 0000-00-00 | No | No | Current |