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END-ZIT
END-ZIT - 68605-2001-2 - (SULFUR)
Drug Information of END-ZIT
| Product NDC: | 68605-2001 |
| Proprietary Name: | END-ZIT |
| Non Proprietary Name: | SULFUR |
| Active Ingredient(s): | .05 g/mL & nbsp; SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION, AUGMENTED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of END-ZIT
| Product NDC: | 68605-2001 |
| Labeler Name: | ABBE Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040420 |
Package Information of END-ZIT
| Package NDC: | 68605-2001-2 |
| Package Description: | 14.78 mL in 1 BOTTLE, GLASS (68605-2001-2) |
NDC Information of END-ZIT
| NDC Code | 68605-2001-2 |
| Proprietary Name | END-ZIT |
| Package Description | 14.78 mL in 1 BOTTLE, GLASS (68605-2001-2) |
| Product NDC | 68605-2001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULFUR |
| Dosage Form Name | LOTION, AUGMENTED |
| Route Name | TOPICAL |
| Start Marketing Date | 20040420 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ABBE Laboratories, Inc. |
| Substance Name | SULFUR |
| Strength Number | .05 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
