Product NDC: | 30142-004 |
Proprietary Name: | Anticavity |
Non Proprietary Name: | Sodium fluoride |
Active Ingredient(s): | 10.4 mg/mL & nbsp; Sodium fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | RINSE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 30142-004 |
Labeler Name: | Kroger Co |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130118 |
Package NDC: | 30142-004-77 |
Package Description: | 500 mL in 1 BOTTLE, PLASTIC (30142-004-77) |
NDC Code | 30142-004-77 |
Proprietary Name | Anticavity |
Package Description | 500 mL in 1 BOTTLE, PLASTIC (30142-004-77) |
Product NDC | 30142-004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium fluoride |
Dosage Form Name | RINSE |
Route Name | ORAL |
Start Marketing Date | 20130118 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kroger Co |
Substance Name | SODIUM FLUORIDE |
Strength Number | 10.4 |
Strength Unit | mg/mL |
Pharmaceutical Classes |