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DELUXE ALL-PURPOSE
DELUXE ALL-PURPOSE - 59854-301-01 - (TRICLOSAN)
Drug Information of DELUXE ALL-PURPOSE
| Product NDC: | 59854-301 |
| Proprietary Name: | DELUXE ALL-PURPOSE |
| Non Proprietary Name: | TRICLOSAN |
| Active Ingredient(s): | 7.57 mL/3.78L & nbsp; TRICLOSAN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DELUXE ALL-PURPOSE
| Product NDC: | 59854-301 |
| Labeler Name: | Johnson Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20000101 |
Package Information of DELUXE ALL-PURPOSE
| Package NDC: | 59854-301-01 |
| Package Description: | 3.78 L in 1 BOTTLE (59854-301-01) |
NDC Information of DELUXE ALL-PURPOSE
| NDC Code | 59854-301-01 |
| Proprietary Name | DELUXE ALL-PURPOSE |
| Package Description | 3.78 L in 1 BOTTLE (59854-301-01) |
| Product NDC | 59854-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TRICLOSAN |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20000101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson Labs, Inc. |
| Substance Name | TRICLOSAN |
| Strength Number | 7.57 |
| Strength Unit | mL/3.78L |
| Pharmaceutical Classes |
