TopSani
- Product NDC
- 24439-321
- 11-digit product format
- 244390321
- Labeler code
- 24439
- Product ID
- 24439-321_4f92100f-6738-4fe2-9360-4b5b7e5e6900
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- United Promotions Inc.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-11-01
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1 mL/1000mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 24439-321-10 | TopSani | 56 mL in 1 BOTTLE, PLASTIC | LIQUID | 56 | | 1 |
| 24439-321-11 | TopSani | 236 mL in 1 BOTTLE, PUMP | LIQUID | 236 | | 1 |
| 24439-321-12 | TopSani | 946 mL in 1 BOTTLE, PLASTIC | LIQUID | 946 | | 1 |
| 24439-321-13 | TopSani | 946 mL in 1 BOTTLE, PUMP | LIQUID | 946 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24439-321 | TOPSANI (BENZALKONIUM CHLORIDE) LIQUID [UNITED PROMOTIONS INC.] | 1 | Legacy NDC, 4 package rows | 20111202_b34b613f-2bda-411c-b988-1ab669e3020d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 24439-321-10 | 24439032110 | 56 mL in 1 BOTTLE, PLASTIC | 56 ml | Historical |
| 24439-321-11 | 24439032111 | 236 mL in 1 BOTTLE, PUMP | 236 ml | Historical |
| 24439-321-12 | 24439032112 | 946 mL in 1 BOTTLE, PLASTIC | 946 ml | Historical |
| 24439-321-13 | 24439032113 | 946 mL in 1 BOTTLE, PUMP | 946 ml | Historical |