ANTIBACTERIAL Hand
- Product NDC
- 78939-001
- 11-digit product format
- 789390001
- Labeler code
- 78939
- Product ID
- 78939-001_74bca929-389f-4da4-988e-c6d2d02233c8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- CROSS BORDER MANUFACTURERS INC.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-16
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 78939-001-01 | ANTIBACTERIAL Hand | 500 mL in 1 BOTTLE, PLASTIC | LIQUID | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78939-001 | ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) LIQUID [CROSS BORDER MANUFACTURERS INC.] | 1 | Legacy NDC, 1 package rows | 20200923_f9ee3405-8dfb-4ffe-8e1b-495f8d1438a7.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 |
|---|
| 78939-001-01 | 78939000101 | 500 mL in 1 BOTTLE, PLASTIC (78939-001-01) | 500 ml | 2020-09-16 | 0000-00-00 | No | No | Current |