Home
>
National Drug Code (NDC)
>
DRY COUGH SKIN ERUPTIONS
DRY COUGH SKIN ERUPTIONS - 64117-227-01 - (EUPHORBIA RESINIFERA RESIN)
Drug Information of DRY COUGH SKIN ERUPTIONS
| Product NDC: | 64117-227 |
| Proprietary Name: | DRY COUGH SKIN ERUPTIONS |
| Non Proprietary Name: | EUPHORBIA RESINIFERA RESIN |
| Active Ingredient(s): | 30 [hp_C]/mL & nbsp; EUPHORBIA RESINIFERA RESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DRY COUGH SKIN ERUPTIONS
| Product NDC: | 64117-227 |
| Labeler Name: | Natural Health Supply |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19980604 |
Package Information of DRY COUGH SKIN ERUPTIONS
| Package NDC: | 64117-227-01 |
| Package Description: | 1.875 mL in 1 BOTTLE, GLASS (64117-227-01) |
NDC Information of DRY COUGH SKIN ERUPTIONS
| NDC Code | 64117-227-01 |
| Proprietary Name | DRY COUGH SKIN ERUPTIONS |
| Package Description | 1.875 mL in 1 BOTTLE, GLASS (64117-227-01) |
| Product NDC | 64117-227 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | EUPHORBIA RESINIFERA RESIN |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 19980604 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Natural Health Supply |
| Substance Name | EUPHORBIA RESINIFERA RESIN |
| Strength Number | 30 |
| Strength Unit | [hp_C]/mL |
| Pharmaceutical Classes |
