NDC 58575-170-80 - AQUACIL
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 58575-170
- Requested NDC
- 58575-170-80
- Package NDCs from labels
- 58575-170-02, 58575-170-80, 58575-170-18, 58575-170-37, 58575-170-10, 58575-170-12
- Manufacturer
- Inopak, Ltd
- Effective date
- 2019-10-30
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AQUACIL - Inopak, Ltd | Inopak, Ltd | 2019-10-30 | HUMAN OTC DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BENZALKONIUM CHLORIDE | ACTIVE INGREDIENT | F5UM2KM3W7 | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| BENZALKONIUM | ACTIVE MOIETY | 7N6JUD5X6Y | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| 1,2-HEXANEDIOL | INACTIVE INGREDIENT | TR046Y3K1G | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| CAPRYLYL GLYCOL | INACTIVE INGREDIENT | 00YIU5438U | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| CETRIMONIUM CHLORIDE | INACTIVE INGREDIENT | UC9PE95IBP | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| CHLORHEXIDINE GLUCONATE | INACTIVE INGREDIENT | MOR84MUD8E | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| PHENOXYETHANOL | INACTIVE INGREDIENT | HIE492ZZ3T | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| POLYQUATERNIUM-10 (125 MPA.S AT 2%) | INACTIVE INGREDIENT | L45WU8S981 | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | AQUACIL (BENZALKONIUM CHLORIDE) LIQUID [INOPAK, LTD] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.