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Crayola
Crayola - 52376-035-02 - (Sodium Fluoride)
Drug Information of Crayola
| Product NDC: | 52376-035 |
| Proprietary Name: | Crayola |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .24 mg/g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Crayola
| Product NDC: | 52376-035 |
| Labeler Name: | Sunstar Americas, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130703 |
Package Information of Crayola
| Package NDC: | 52376-035-02 |
| Package Description: | 3 TUBE in 1 CARTON (52376-035-02) > 42.5 g in 1 TUBE |
NDC Information of Crayola
| NDC Code | 52376-035-02 |
| Proprietary Name | Crayola |
| Package Description | 3 TUBE in 1 CARTON (52376-035-02) > 42.5 g in 1 TUBE |
| Product NDC | 52376-035 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20130703 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sunstar Americas, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .24 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
