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RENEWAL
RENEWAL - 11822-2108-0 - (TRICLOSAN)
Drug Information of RENEWAL
| Product NDC: | 11822-2108 |
| Proprietary Name: | RENEWAL |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | .115 L/100L & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RENEWAL
| Product NDC: | 11822-2108 |
| Labeler Name: | RITE AID |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110318 |
Package Information of RENEWAL
| Package NDC: | 11822-2108-0 |
| Package Description: | 2.36 L in 1 BOTTLE (11822-2108-0) |
NDC Information of RENEWAL
| NDC Code | 11822-2108-0 |
| Proprietary Name | RENEWAL |
| Package Description | 2.36 L in 1 BOTTLE (11822-2108-0) |
| Product NDC | 11822-2108 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110318 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | RITE AID |
| Substance Name | TRICLOSAN |
| Strength Number | .115 |
| Strength Unit | L/100L |
| Pharmaceutical Classes |
