Delphis Eco
- Product NDC
- 81560-002
- 11-digit product format
- 815600002
- Labeler code
- 81560
- Product ID
- 81560-002_ba9a6122-b05a-2358-e053-2995a90a43d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- DELPHIS ECO LIMITED
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-02-23
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 3 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 |
|---|
| 81560-002-05 | Delphis Eco | 500 mL in 1 BOTTLE, SPRAY | LIQUID | 500 | | 1 |
| 81560-002-07 | Delphis Eco | 700 mL in 1 BOTTLE, SPRAY | LIQUID | 700 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81560-002 | DELPHIS ECO HAND SANITISING FOAM (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO (BENZALKONIUM CHLORIDE) LIQUID DELPHIS ECO HAND SANITISER (BENZALKONIUM CHLORIDE) LIQUID [DELPHIS ECO LIMITED] | 1 | Legacy NDC, 2 package rows | 20210227_ba9a6122-b059-2358-e053-2995a90a43d4.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 |
|---|
| 81560-002-05 | 81560000205 | 500 mL in 1 BOTTLE, SPRAY (81560-002-05) | 500 ml | 2021-02-23 | 0000-00-00 | No | No | Current |
| 81560-002-07 | 81560000207 | 700 mL in 1 BOTTLE, SPRAY (81560-002-07) | 700 ml | 2021-02-23 | 0000-00-00 | No | No | Current |