INOFOAM Antibacterial
- Product NDC
- 58575-526
- 11-digit product format
- 585750526
- Labeler code
- 58575
- Product ID
- 58575-526_e29c3814-4b81-6b21-e053-2a95a90a6ed1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Inopak, Ltd
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-06-29
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 58575-526-01 | INOFOAM AntibacterialFoaming Hand Wash | 1000 mL in 1 POUCH | LIQUID | 1000 | | 1 |
| 58575-526-42 | INOFOAM AntibacterialFoaming Hand Wash | 3785 mL in 1 JUG | LIQUID | 3785 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58575-526 | INOFOAM ANTIBACTERIAL FOAMING HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | Legacy NDC, 2 package rows | 20220702_e29c3814-4b82-6b21-e053-2a95a90a6ed1.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 |
|---|
| 58575-526-01 | 58575052601 | 1000 mL in 1 POUCH (58575-526-01) | 1000 ml | 2022-06-29 | 0000-00-00 | No | No | Current |
| 58575-526-42 | 58575052642 | 3785 mL in 1 JUG (58575-526-42) | 3785 ml | 2022-06-29 | 0000-00-00 | No | No | Current |