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HEB
HEB - 37808-192-00 - (Fluoride)
Drug Information of HEB
| Product NDC: | 37808-192 |
| Proprietary Name: | HEB |
| Non Proprietary Name: | Fluoride |
| Active Ingredient(s): | .243 g/100g & nbsp; Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HEB
| Product NDC: | 37808-192 |
| Labeler Name: | HEB |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121201 |
Package Information of HEB
| Package NDC: | 37808-192-00 |
| Package Description: | 12 TUBE in 1 CASE (37808-192-00) > 120 g in 1 TUBE (37808-192-02) |
NDC Information of HEB
| NDC Code | 37808-192-00 |
| Proprietary Name | HEB |
| Package Description | 12 TUBE in 1 CASE (37808-192-00) > 120 g in 1 TUBE (37808-192-02) |
| Product NDC | 37808-192 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HEB |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .243 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
