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SheerFluorX
SheerFluorX - 14060-005-04 - (sodium fluoride)
Drug Information of SheerFluorX
| Product NDC: | 14060-005 |
| Proprietary Name: | SheerFluorX |
| Non Proprietary Name: | sodium fluoride |
| Active Ingredient(s): | 20 mg/1 & nbsp; sodium fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | FILM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SheerFluorX
| Product NDC: | 14060-005 |
| Labeler Name: | CAO Group, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100901 |
Package Information of SheerFluorX
| Package NDC: | 14060-005-04 |
| Package Description: | 4 TRAY in 1 PACKAGE (14060-005-04) > 2 FILM in 1 TRAY |
NDC Information of SheerFluorX
| NDC Code | 14060-005-04 |
| Proprietary Name | SheerFluorX |
| Package Description | 4 TRAY in 1 PACKAGE (14060-005-04) > 2 FILM in 1 TRAY |
| Product NDC | 14060-005 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sodium fluoride |
| Dosage Form Name | FILM |
| Route Name | DENTAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | CAO Group, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
