Product NDC: | 37000-833 |
Proprietary Name: | Kids Crest |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | .22 mg/mL & nbsp; Sodium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | RINSE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-833 |
Labeler Name: | Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120723 |
Package NDC: | 37000-833-01 |
Package Description: | 500 mL in 1 BOTTLE, PLASTIC (37000-833-01) |
NDC Code | 37000-833-01 |
Proprietary Name | Kids Crest |
Package Description | 500 mL in 1 BOTTLE, PLASTIC (37000-833-01) |
Product NDC | 37000-833 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | RINSE |
Route Name | ORAL |
Start Marketing Date | 20120723 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Procter & Gamble Manufacturing Company |
Substance Name | SODIUM FLUORIDE |
Strength Number | .22 |
Strength Unit | mg/mL |
Pharmaceutical Classes |