| Product NDC: | 57955-5082 |
| Proprietary Name: | Vaccinoplex |
| Non Proprietary Name: | Aconitum napellus, Apis mellifica, Chamomilla, Hypericum perforatum, Ledum palustre, Pulsatilla, Silicea, Thuja occidentalis |
| Active Ingredient(s): | 10; 10; 10; 10; 10; 10; 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL & nbsp; Aconitum napellus, Apis mellifica, Chamomilla, Hypericum perforatum, Ledum palustre, Pulsatilla, Silicea, Thuja occidentalis |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57955-5082 |
| Labeler Name: | King Bio Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111026 |
| Package NDC: | 57955-5082-2 |
| Package Description: | 59 mL in 1 BOTTLE, SPRAY (57955-5082-2) |
| NDC Code | 57955-5082-2 |
| Proprietary Name | Vaccinoplex |
| Package Description | 59 mL in 1 BOTTLE, SPRAY (57955-5082-2) |
| Product NDC | 57955-5082 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aconitum napellus, Apis mellifica, Chamomilla, Hypericum perforatum, Ledum palustre, Pulsatilla, Silicea, Thuja occidentalis |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111026 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | King Bio Inc. |
| Substance Name | APIS MELLIFERA; HYPERICUM PERFORATUM; LEDUM PALUSTRE TWIG; MATRICARIA RECUTITA; PULSATILLA VULGARIS; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAFY TWIG |
| Strength Number | 10; 10; 10; 10; 10; 10; 10 |
| Strength Unit | [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |
| Pharmaceutical Classes |