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Osteodoron PM Bone Support
Osteodoron PM Bone Support - 48951-7097-4 - (OYSTER SHELL CALCIUM CARBONATE, CRUDE WHITE OAK BARK CALCIUM FLUORIDE SILICON DIOXIDE)
Drug Information of Osteodoron PM Bone Support
| Product NDC: | 48951-7097 |
| Proprietary Name: | Osteodoron PM Bone Support |
| Non Proprietary Name: | OYSTER SHELL CALCIUM CARBONATE, CRUDE WHITE OAK BARK CALCIUM FLUORIDE SILICON DIOXIDE |
| Active Ingredient(s): | 6; 1; 6; 4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; OYSTER SHELL CALCIUM CARBONATE, CRUDE WHITE OAK BARK CALCIUM FLUORIDE SILICON DIOXIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Osteodoron PM Bone Support
| Product NDC: | 48951-7097 |
| Labeler Name: | Uriel Pharmacy Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20090901 |
Package Information of Osteodoron PM Bone Support
| Package NDC: | 48951-7097-4 |
| Package Description: | 1 POWDER in 1 BOTTLE, GLASS (48951-7097-4) |
NDC Information of Osteodoron PM Bone Support
| NDC Code | 48951-7097-4 |
| Proprietary Name | Osteodoron PM Bone Support |
| Package Description | 1 POWDER in 1 BOTTLE, GLASS (48951-7097-4) |
| Product NDC | 48951-7097 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OYSTER SHELL CALCIUM CARBONATE, CRUDE WHITE OAK BARK CALCIUM FLUORIDE SILICON DIOXIDE |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Uriel Pharmacy Inc |
| Substance Name | CALCIUM FLUORIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SILICON DIOXIDE; WHITE OAK BARK |
| Strength Number | 6; 1; 6; 4 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |
