Product NDC: | 29500-2238 |
Proprietary Name: | Advanced Whitening Anticavity Fluoride |
Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 29500-2238 |
Labeler Name: | Personal Care Products, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110124 |
Package NDC: | 29500-2238-6 |
Package Description: | 1 TUBE in 1 BOX (29500-2238-6) > 181 g in 1 TUBE |
NDC Code | 29500-2238-6 |
Proprietary Name | Advanced Whitening Anticavity Fluoride |
Package Description | 1 TUBE in 1 BOX (29500-2238-6) > 181 g in 1 TUBE |
Product NDC | 29500-2238 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
Dosage Form Name | PASTE, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20110124 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Personal Care Products, LLC |
Substance Name | SODIUM MONOFLUOROPHOSPHATE |
Strength Number | .76 |
Strength Unit | g/100g |
Pharmaceutical Classes |