| Product NDC: | 61995-0302 |
| Proprietary Name: | Jason Dandruff Relief Treatment |
| Non Proprietary Name: | Sulfur, Salicylic Acid |
| Active Ingredient(s): | 2; 2 g/100g; g/100g & nbsp; Sulfur, Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61995-0302 |
| Labeler Name: | The Hain Celestial Group, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100105 |
| Package NDC: | 61995-0302-2 |
| Package Description: | 355 g in 1 BOTTLE (61995-0302-2) |
| NDC Code | 61995-0302-2 |
| Proprietary Name | Jason Dandruff Relief Treatment |
| Package Description | 355 g in 1 BOTTLE (61995-0302-2) |
| Product NDC | 61995-0302 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sulfur, Salicylic Acid |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20100105 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Hain Celestial Group, Inc |
| Substance Name | SALICYLIC ACID; SULFUR |
| Strength Number | 2; 2 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |