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Dawn
Dawn - 37000-606-29 - (Triclosan)
Drug Information of Dawn
| Product NDC: | 37000-606 |
| Proprietary Name: | Dawn |
| Non Proprietary Name: | Triclosan |
| Active Ingredient(s): | .1 g/100mL & nbsp; Triclosan |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dawn
| Product NDC: | 37000-606 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110201 |
Package Information of Dawn
| Package NDC: | 37000-606-29 |
| Package Description: | 857 mL in 1 BOTTLE, PLASTIC (37000-606-29) |
NDC Information of Dawn
| NDC Code | 37000-606-29 |
| Proprietary Name | Dawn |
| Package Description | 857 mL in 1 BOTTLE, PLASTIC (37000-606-29) |
| Product NDC | 37000-606 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Triclosan |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20110201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | TRICLOSAN |
| Strength Number | .1 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
