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Coniferyl Alcohol
Coniferyl Alcohol - 43742-0185-1 - (Coniferyl Alcohol)
Drug Information of Coniferyl Alcohol
| Product NDC: | 43742-0185 |
| Proprietary Name: | Coniferyl Alcohol |
| Non Proprietary Name: | Coniferyl Alcohol |
| Active Ingredient(s): | 6 [hp_X]/mL & nbsp; Coniferyl Alcohol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Coniferyl Alcohol
| Product NDC: | 43742-0185 |
| Labeler Name: | Deseret Biologicals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20121029 |
Package Information of Coniferyl Alcohol
| Package NDC: | 43742-0185-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (43742-0185-1) |
NDC Information of Coniferyl Alcohol
| NDC Code | 43742-0185-1 |
| Proprietary Name | Coniferyl Alcohol |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-0185-1) |
| Product NDC | 43742-0185 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Coniferyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20121029 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Deseret Biologicals, Inc. |
| Substance Name | CONIFERYL ALCOHOL |
| Strength Number | 6 |
| Strength Unit | [hp_X]/mL |
| Pharmaceutical Classes |
