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SunDrops 77
SunDrops 77 - 63621-354-85 - (Benzalkonium Chloride)
Drug Information of SunDrops 77
| Product NDC: | 63621-354 |
| Proprietary Name: | SunDrops 77 |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SunDrops 77
| Product NDC: | 63621-354 |
| Labeler Name: | Sunburst Chemicals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080505 |
Package Information of SunDrops 77
| Package NDC: | 63621-354-85 |
| Package Description: | 8 BAG in 1 BOX (63621-354-85) > 1000 mL in 1 BAG |
NDC Information of SunDrops 77
| NDC Code | 63621-354-85 |
| Proprietary Name | SunDrops 77 |
| Package Description | 8 BAG in 1 BOX (63621-354-85) > 1000 mL in 1 BAG |
| Product NDC | 63621-354 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20080505 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sunburst Chemicals, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
