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FluoriSHIELD
FluoriSHIELD - 10733-130-04 - (Sodium Fluoride)
Drug Information of FluoriSHIELD
| Product NDC: | 10733-130 |
| Proprietary Name: | FluoriSHIELD |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 11 mg/g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FluoriSHIELD
| Product NDC: | 10733-130 |
| Labeler Name: | Medical Products Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091129 |
Package Information of FluoriSHIELD
| Package NDC: | 10733-130-04 |
| Package Description: | 66 BOTTLE in 1 CARTON (10733-130-04) > 114 g in 1 BOTTLE |
NDC Information of FluoriSHIELD
| NDC Code | 10733-130-04 |
| Proprietary Name | FluoriSHIELD |
| Package Description | 66 BOTTLE in 1 CARTON (10733-130-04) > 114 g in 1 BOTTLE |
| Product NDC | 10733-130 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | GEL |
| Route Name | DENTAL |
| Start Marketing Date | 20091129 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Medical Products Laboratories, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 11 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
