| Product NDC: | 42346-500 |
| Proprietary Name: | Frankincense and Myrrh Sciatica |
| Non Proprietary Name: | Aconitum napellus, Bryonia alba, Hypericum perforatum |
| Active Ingredient(s): | 3; 3; 3 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL & nbsp; Aconitum napellus, Bryonia alba, Hypericum perforatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OIL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42346-500 |
| Labeler Name: | Wise Consumer Products Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130402 |
| Package NDC: | 42346-500-59 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (42346-500-59) > 59 mL in 1 BOTTLE, DROPPER |
| NDC Code | 42346-500-59 |
| Proprietary Name | Frankincense and Myrrh Sciatica |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (42346-500-59) > 59 mL in 1 BOTTLE, DROPPER |
| Product NDC | 42346-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aconitum napellus, Bryonia alba, Hypericum perforatum |
| Dosage Form Name | OIL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130402 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Wise Consumer Products Co. |
| Substance Name | ACONITUM NAPELLUS; BRYONIA ALBA ROOT; HYPERICUM PERFORATUM |
| Strength Number | 3; 3; 3 |
| Strength Unit | [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
| Pharmaceutical Classes |