Native Green Foaming Hand Sanitizer
- Product NDC
- 50409-514
- 11-digit product format
- 504090514
- Labeler code
- 50409
- Product ID
- 50409-514_86f6b0d9-e0f9-4042-9e9c-62607f7679c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Native Green
- Application
- part333
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-04-21
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 g/1000mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 50409-514-42 | Native Green Foaming Hand Sanitizer | 50 mL in 1 BOTTLE | SOLUTION | 50 | | 1 |
| 50409-514-82 | Native Green Foaming Hand Sanitizer | 550 mL in 1 BOTTLE | SOLUTION | 550 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50409-514 | NATIVE GREEN FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [NATIVE GREEN] | 1 | Legacy NDC, 2 package rows | 20100510_75c243a8-242c-4ca1-a983-89f07aec3041.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50409-514-42 | 50409051442 | 50 mL in 1 BOTTLE | 50 ml | Historical |
| 50409-514-82 | 50409051482 | 550 mL in 1 BOTTLE | 550 ml | Historical |