Zoviro
- Product NDC
- 83814-006
- 11-digit product format
- 838140006
- Labeler code
- 83814
- Product ID
- 83814-006_40844d7d-3a50-ce94-e063-6294a90a7fa7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Zoviro, LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-04-21
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .12 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zoviro
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .12 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1046310 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83814-006-01 | Zoviro | 281 mL in 1 BOTTLE, PUMP | LIQUID | 281 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83814-006 | ZOVIRO (BENZALKONIUM CHLORIDE) LIQUID [ZOVIRO, LLC] | 1 | Current NDC, 1 package rows | 20250430_33e1e96d-1058-35d5-e063-6394a90a4c9e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 83814-006-01 | 83814000601 | 281 mL in 1 BOTTLE, PUMP (83814-006-01) | 281 ml | 2025-04-21 | No | No | Historical |