| Product NDC: | 54897-507 |
| Proprietary Name: | Topical Fluoride Foam Bumble Bee Bubble Gum |
| Non Proprietary Name: | Acidulated Phosphate Fluoride |
| Active Ingredient(s): | 2.3; 10 mg/g; mg/g & nbsp; Acidulated Phosphate Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | AEROSOL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54897-507 |
| Labeler Name: | Laclede, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000504 |
| Package NDC: | 54897-507-17 |
| Package Description: | 165 g in 1 BOTTLE (54897-507-17) |
| NDC Code | 54897-507-17 |
| Proprietary Name | Topical Fluoride Foam Bumble Bee Bubble Gum |
| Package Description | 165 g in 1 BOTTLE (54897-507-17) |
| Product NDC | 54897-507 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acidulated Phosphate Fluoride |
| Dosage Form Name | AEROSOL |
| Route Name | DENTAL |
| Start Marketing Date | 20000504 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Laclede, Inc. |
| Substance Name | HYDROFLUORIC ACID; SODIUM FLUORIDE |
| Strength Number | 2.3; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |