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Oral-B
Oral-B - 0041-1421-16 - (Sodium Fluoride)
Drug Information of Oral-B
| Product NDC: | 0041-1421 |
| Proprietary Name: | Oral-B |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 500 ug/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oral-B
| Product NDC: | 0041-1421 |
| Labeler Name: | Oral-B Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20051015 |
Package Information of Oral-B
| Package NDC: | 0041-1421-16 |
| Package Description: | 500 mL in 1 BOTTLE, PLASTIC (0041-1421-16) |
NDC Information of Oral-B
| NDC Code | 0041-1421-16 |
| Proprietary Name | Oral-B |
| Package Description | 500 mL in 1 BOTTLE, PLASTIC (0041-1421-16) |
| Product NDC | 0041-1421 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | LIQUID |
| Route Name | DENTAL |
| Start Marketing Date | 20051015 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Oral-B Laboratories |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 500 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes |
