CVS Merthiolate
- Product NDC
- 69842-749
- 11-digit product format
- 698420749
- Labeler code
- 69842
- Product ID
- 69842-749_0d19a0a5-ed0c-1796-e063-6294a90a7e8f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- CVS Pharmacy
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2008-01-01
- 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
- CVS 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 |
|---|
| 69842-749-92 | CVS Merthiolate | 59 mL in 1 BOTTLE, PLASTIC | LIQUID | 59 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-749 | CVS MERTHIOLATE (BENZALKONIUM CHLORIDE) LIQUID [CVS PHARMACY] | 5 | Current NDC, Legacy NDC, 1 package rows | 20231223_dd498ab1-8350-41aa-86fc-2db57005f3e2.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 |
|---|
| 69842-749-92 | 69842074992 | 59 mL in 1 BOTTLE, PLASTIC (69842-749-92) | 59 ml | 2008-01-01 | 0000-00-00 | No | No | Current |