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Be-Dry
Be-Dry - 68703-003-80 - (Equisetum arv)
Drug Information of Be-Dry
| Product NDC: | 68703-003 |
| Proprietary Name: | Be-Dry |
| Non Proprietary Name: | Equisetum arv |
| Active Ingredient(s): | 6 [hp_C]/1 & nbsp; Equisetum arv |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Be-Dry
| Product NDC: | 68703-003 |
| Labeler Name: | Native Remedies, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130102 |
Package Information of Be-Dry
| Package NDC: | 68703-003-80 |
| Package Description: | 180 TABLET in 1 BOTTLE, GLASS (68703-003-80) |
NDC Information of Be-Dry
| NDC Code | 68703-003-80 |
| Proprietary Name | Be-Dry |
| Package Description | 180 TABLET in 1 BOTTLE, GLASS (68703-003-80) |
| Product NDC | 68703-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Equisetum arv |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130102 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Native Remedies, LLC |
| Substance Name | EQUISETUM ARVENSE TOP |
| Strength Number | 6 |
| Strength Unit | [hp_C]/1 |
| Pharmaceutical Classes |
