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Ulta Nectarine Spice Anti-Bacterial Gentle Foaming
Ulta Nectarine Spice Anti-Bacterial Gentle Foaming - 62296-0027-1 - (Triclosan)
Drug Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming
| Product NDC: | 62296-0027 |
| Proprietary Name: | Ulta Nectarine Spice Anti-Bacterial Gentle Foaming |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .3 g/100g & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming
| Product NDC: | 62296-0027 |
| Labeler Name: | Ulta |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120601 |
Package Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming
| Package NDC: | 62296-0027-1 |
| Package Description: | 242 g in 1 BOTTLE, PLASTIC (62296-0027-1) |
NDC Information of Ulta Nectarine Spice Anti-Bacterial Gentle Foaming
| NDC Code | 62296-0027-1 |
| Proprietary Name | Ulta Nectarine Spice Anti-Bacterial Gentle Foaming |
| Package Description | 242 g in 1 BOTTLE, PLASTIC (62296-0027-1) |
| Product NDC | 62296-0027 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ulta |
| Substance Name | TRICLOSAN |
| Strength Number | .3 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
