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 |