Product NDC: | 10237-630 |
Proprietary Name: | AIM |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | 2.4 mg/g & nbsp; Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10237-630 |
Labeler Name: | Church & Dwight Co., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101110 |
Package NDC: | 10237-630-60 |
Package Description: | 1 TUBE in 1 CARTON (10237-630-60) > 170 g in 1 TUBE |
NDC Code | 10237-630-60 |
Proprietary Name | AIM |
Package Description | 1 TUBE in 1 CARTON (10237-630-60) > 170 g in 1 TUBE |
Product NDC | 10237-630 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 20101110 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Church & Dwight Co., Inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | 2.4 |
Strength Unit | mg/g |
Pharmaceutical Classes |