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Hello Kitty
Hello Kitty - 64893-310-01 - (SODIUM FLUORIDE)
Drug Information of Hello Kitty
| Product NDC: | 64893-310 |
| Proprietary Name: | Hello Kitty |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .243 g/100g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hello Kitty
| Product NDC: | 64893-310 |
| Labeler Name: | Dr. Fresh, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110620 |
Package Information of Hello Kitty
| Package NDC: | 64893-310-01 |
| Package Description: | 1 TUBE in 1 PACKAGE (64893-310-01) > 24 g in 1 TUBE |
NDC Information of Hello Kitty
| NDC Code | 64893-310-01 |
| Proprietary Name | Hello Kitty |
| Package Description | 1 TUBE in 1 PACKAGE (64893-310-01) > 24 g in 1 TUBE |
| Product NDC | 64893-310 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20110620 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dr. Fresh, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .243 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
