Product NDC: | 37000-004 |
Proprietary Name: | Crest Pro-Health |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | .0219 g/mL & nbsp; Sodium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | RINSE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-004 |
Labeler Name: | Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100816 |
Package NDC: | 37000-004-02 |
Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (37000-004-02) |
NDC Code | 37000-004-02 |
Proprietary Name | Crest Pro-Health |
Package Description | 1000 mL in 1 BOTTLE, PLASTIC (37000-004-02) |
Product NDC | 37000-004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | RINSE |
Route Name | ORAL |
Start Marketing Date | 20100816 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Procter & Gamble Manufacturing Company |
Substance Name | SODIUM FLUORIDE |
Strength Number | .0219 |
Strength Unit | g/mL |
Pharmaceutical Classes |