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fiteBac SkinCare
fiteBac SkinCare - 13136-001-01 - (Benzalkonium Chloride)
Drug Information of fiteBac SkinCare
| Product NDC: | 13136-001 |
| Proprietary Name: | fiteBac SkinCare |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .029 mL/29.57mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of fiteBac SkinCare
| Product NDC: | 13136-001 |
| Labeler Name: | fiteBac SkinCare, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111115 |
Package Information of fiteBac SkinCare
| Package NDC: | 13136-001-01 |
| Package Description: | 29.57 mL in 1 TUBE (13136-001-01) |
NDC Information of fiteBac SkinCare
| NDC Code | 13136-001-01 |
| Proprietary Name | fiteBac SkinCare |
| Package Description | 29.57 mL in 1 TUBE (13136-001-01) |
| Product NDC | 13136-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20111115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | fiteBac SkinCare, LLC |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .029 |
| Strength Unit | mL/29.57mL |
| Pharmaceutical Classes |
