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Solmeet
Solmeet - 42352-3001-1 - (calcium carbonate)
Drug Information of Solmeet
| Product NDC: | 42352-3001 |
| Proprietary Name: | Solmeet |
| Non Proprietary Name: | calcium carbonate |
| Active Ingredient(s): | .05; .05; 15.85; .6 g/100g; g/100g; g/100g; g/100g & nbsp; calcium carbonate |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Solmeet
| Product NDC: | 42352-3001 |
| Labeler Name: | Solbin Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101215 |
Package Information of Solmeet
| Package NDC: | 42352-3001-1 |
| Package Description: | 120 g in 1 TUBE (42352-3001-1) |
NDC Information of Solmeet
| NDC Code | 42352-3001-1 |
| Proprietary Name | Solmeet |
| Package Description | 120 g in 1 TUBE (42352-3001-1) |
| Product NDC | 42352-3001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | calcium carbonate |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20101215 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Solbin Co., Ltd |
| Substance Name | ALCLOXA; AMINOCAPROIC ACID; CALCIUM CARBONATE; DIBASIC CALCIUM PHOSPHATE DIHYDRATE |
| Strength Number | .05; .05; 15.85; .6 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
