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Plus White Xtra Whitening
Plus White Xtra Whitening - 61543-7243-3 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of Plus White Xtra Whitening
| Product NDC: | 61543-7243 |
| Proprietary Name: | Plus White Xtra Whitening |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .884 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Plus White Xtra Whitening
| Product NDC: | 61543-7243 |
| Labeler Name: | CCA Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100611 |
Package Information of Plus White Xtra Whitening
| Package NDC: | 61543-7243-3 |
| Package Description: | 1 TUBE in 1 BOX (61543-7243-3) > 100 g in 1 TUBE |
NDC Information of Plus White Xtra Whitening
| NDC Code | 61543-7243-3 |
| Proprietary Name | Plus White Xtra Whitening |
| Package Description | 1 TUBE in 1 BOX (61543-7243-3) > 100 g in 1 TUBE |
| Product NDC | 61543-7243 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20100611 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CCA Industries, Inc. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .884 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
