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Sucrets Complete - 63736-920-18 - (Dyclonine Hydrochloride and Menthol)
Drug Information of Sucrets Complete
| Product NDC: | 63736-920 |
| Proprietary Name: | Sucrets Complete |
| Non Proprietary Name: | Dyclonine Hydrochloride and Menthol |
| Active Ingredient(s): | 3; 6 mg/1; mg/1 & nbsp; Dyclonine Hydrochloride and Menthol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sucrets Complete
| Product NDC: | 63736-920 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090731 |
Package Information of Sucrets Complete
| Package NDC: | 63736-920-18 |
| Package Description: | 18 LOZENGE in 1 CANISTER (63736-920-18) |
NDC Information of Sucrets Complete
| NDC Code | 63736-920-18 |
| Proprietary Name | Sucrets Complete |
| Package Description | 18 LOZENGE in 1 CANISTER (63736-920-18) |
| Product NDC | 63736-920 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dyclonine Hydrochloride and Menthol |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20090731 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | DYCLONINE HYDROCHLORIDE; MENTHOL |
| Strength Number | 3; 6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
