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kolorz
kolorz - 10733-372-00 - (Sodium Fluoride)
Drug Information of kolorz
| Product NDC: | 10733-372 |
| Proprietary Name: | kolorz |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 27.2 mg/g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of kolorz
| Product NDC: | 10733-372 |
| Labeler Name: | Medical Products Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070101 |
Package Information of kolorz
| Package NDC: | 10733-372-00 |
| Package Description: | 6 CAN in 1 BOX (10733-372-00) > 125 g in 1 CAN |
NDC Information of kolorz
| NDC Code | 10733-372-00 |
| Proprietary Name | kolorz |
| Package Description | 6 CAN in 1 BOX (10733-372-00) > 125 g in 1 CAN |
| Product NDC | 10733-372 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | DENTAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Medical Products Laboratories, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 27.2 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
