Tincture Merthiolate
- Product NDC
- 24286-1532
- 11-digit product format
- 242861532
- Labeler code
- 24286
- Product ID
- 24286-1532_0ccb3e8a-3cff-1364-e063-6294a90a70e8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- TINCTURE
- Route
- TOPICAL
- Labeler
- DLC Laboratories, Inc
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-03-22
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 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
- Tincture Merthiolate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1049254 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24286-1532-7 | Tincture Merthiolate | 30 mL in 1 BOTTLE | TINCTURE | 30 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24286-1532 | TINCTURE MERTHIOLATE (BENZALKONIUM CHLORIDE) TINCTURE [DLC LABORATORIES, INC] | 8 | Current NDC, Legacy NDC, 1 package rows | 20231219_4fec9119-fbbf-4fc7-9122-c6300cac8731.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 |
|---|
| 24286-1532-7 | 24286153207 | 30 mL in 1 BOTTLE (24286-1532-7) | 30 ml | 2017-12-13 | 0000-00-00 | No | No | Current |