Search by Drug Name or NDC
NDC 64616-0082-02 Category I 6; 6; 15; 17; 14; 5; 10; 10; 10; 10; 7; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details
Category I 6; 6; 15; 17; 14; 5; 10; 10; 10; 10; 7; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Category I is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Vitality Works, Inc. The primary component is ACTAEA SPICATA ROOT; ANAGALLIS ARVENSIS; ARGEMONE MEXICANA; CANDIDA ALBICANS; HELODERMA HORRIDUM VENOM; HYOSCYAMUS NIGER; POTASSIUM DICHROMATE; POTASSIUM IODIDE; POTASSIUM NITRATE; POTASSIUM PHOSPHATE, DIBASIC; SENNA LEAF; SPONGIA OFFICINALIS SKELETON, RO.
Product Information
NDC | 64616-0082 |
---|---|
Product ID | 64616-082_0d9b708d-7035-1072-e063-6394a90a7f2c |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Category I |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Immune System Booster |
Product Type | HUMAN OTC DRUG |
Dosage Form | LIQUID |
Route | ORAL |
Active Ingredient Strength | 6; 6; 15; 17; 14; 5; 10; 10; 10; 10; 7; 15 |
Active Ingredient Units | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Substance Name | ACTAEA SPICATA ROOT; ANAGALLIS ARVENSIS; ARGEMONE MEXICANA; CANDIDA ALBICANS; HELODERMA HORRIDUM VENOM; HYOSCYAMUS NIGER; POTASSIUM DICHROMATE; POTASSIUM IODIDE; POTASSIUM NITRATE; POTASSIUM PHOSPHATE, DIBASIC; SENNA LEAF; SPONGIA OFFICINALIS SKELETON, RO |
Labeler Name | Vitality Works, Inc |
Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC] |
DEA Schedule | n/a |
Marketing Category | UNAPPROVED HOMEOPATHIC |
Application Number | n/a |
Listing Certified Through | 2024-12-31 |
Package
NDC 64616-0082-02 (64616008202)
NDC Package Code | 64616-082-02 |
---|---|
Billing NDC | 64616008202 |
Package | 59 mL in 1 BOTTLE, DROPPER (64616-082-02) |
Marketing Start Date | 2013-04-16 |
NDC Exclude Flag | N |
Pricing Information | N/A |