Zoviro
- Product NDC
- 83814-005
- 11-digit product format
- 838140005
- Labeler code
- 83814
- Product ID
- 83814-005_40844d7d-3a4d-ce94-e063-6294a90a7fa7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Zoviro, LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-01-09
- Substance
- ALCOHOL
- Active strength
- 70 mL/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 |
|---|
| ALCOHOL | 70 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 582753 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83814-005-01 | Zoviro | 60 mL in 1 BOTTLE | LIQUID | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83814-005 | ZOVIRO (ALCOHOL) LIQUID [ZOVIRO, LLC] | 2 | Current NDC, 1 package rows | 20250205_0e85fb58-7cca-8ae3-e063-6294a90a2553.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 |
|---|
| 83814-005-01 | 83814000501 | 60 mL in 1 BOTTLE (83814-005-01) | 60 ml | 2024-01-09 | No | No | Historical |