Quality Choice Merthiolate
- Product NDC
- 63868-493
- 11-digit product format
- 638680493
- Labeler code
- 63868
- Product ID
- 63868-493_0cf4bfe6-3853-e836-e063-6394a90ab8c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Chain Drug Market Association
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1998-03-25
- 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
- Quality Choice 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 |
|---|
| 63868-493-02 | Quality Choice Merthiolate | 59 mL in 1 BOTTLE | LIQUID | 59 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-493 | QUALITY CHOICE MERTHIOLATE (BENZALKONIUM CHLORIDE) LIQUID [CHAIN DRUG MARKET ASSOCIATION] | 5 | Current NDC, Legacy NDC, 1 package rows | 20231221_5b7303b9-b8c4-4e7c-876f-70ed76443055.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 |
|---|
| 63868-493-02 | 63868049302 | 59 mL in 1 BOTTLE (63868-493-02) | 59 ml | 2017-12-12 | 0000-00-00 | No | No | Current |