Product NDC: | 59883-642 |
Proprietary Name: | Kids Kare |
Non Proprietary Name: | Kids Kare |
Active Ingredient(s): | 4.3 mg/g & nbsp; Kids Kare |
Administration Route(s): | ORAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59883-642 |
Labeler Name: | Zila Therapeutics, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20081121 |
Package NDC: | 59883-642-04 |
Package Description: | 122 g in 1 TUBE (59883-642-04) |
NDC Code | 59883-642-04 |
Proprietary Name | Kids Kare |
Package Description | 122 g in 1 TUBE (59883-642-04) |
Product NDC | 59883-642 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Kids Kare |
Dosage Form Name | GEL |
Route Name | ORAL |
Start Marketing Date | 20081121 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Zila Therapeutics, Inc. |
Substance Name | STANNOUS FLUORIDE |
Strength Number | 4.3 |
Strength Unit | mg/g |
Pharmaceutical Classes |