ViroCLEAR
- Product NDC
- 81909-0001
- 11-digit product format
- 819090001
- Labeler code
- 81909
- Product ID
- 81909-0001_c42cd186-6b91-3e3a-e053-2a95a90a651c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Bioinnovate Pty Ltd
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-06-07
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81909-0001-1 | ViroCLEAR | 50 mL in 1 BOTTLE, SPRAY | LIQUID | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81909-0001 | VIROCLEAR (BENZALKONIUM CHLORIDE) LIQUID [BIOINNOVATE PTY LTD] | 1 | Legacy NDC, 1 package rows | 20210608_c42cd186-6b90-3e3a-e053-2a95a90a651c.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 |
|---|
| 81909-0001-1 | 81909000101 | 50 mL in 1 BOTTLE, SPRAY (81909-0001-1) | 50 ml | 2021-06-07 | 0000-00-00 | No | No | Current |