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NDC 43742-2089-01 Control 12; 12; 12; 6; 6; 6; 12; 12; 12; 6; 6; 6; 12; 6; 8; 8; 12; 12; 12; 6 [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; [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
Control 12; 12; 12; 6; 6; 6; 12; 12; 12; 6; 6; 6; 12; 6; 8; 8; 12; 12; 12; 6 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Control is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Deseret Biologicals, Inc.. The primary component is ASARUM CANADENSE ROOT; BLATTA ORIENTALIS; BUFO BUFO CUTANEOUS GLAND; CLEMATIS RECTA FLOWERING TOP; CUPRIC ACETATE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; SODIUM CHLORIDE; SODIUM .
Product Information
NDC | 43742-2089 |
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Product ID | 43742-2089_6bac1cc6-55be-4c8e-afe8-407c8675d08a |
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 | Control |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Anacardium Orientale, Aqua Marina, Argentum Nitricum, Asarum Canadense, Blatta Orientalis, Bufo Rana, Cerebrum Suis, Clematis Erecta, Cuprum Aceticum, Hypothalamus Suis, Ignatia Amara, Kali Phosphoricum, Lachesis Mutus, Mercurius Solubilis, Natrum Sulphur |
Product Type | HUMAN OTC DRUG |
Dosage Form | LIQUID |
Route | ORAL |
Active Ingredient Strength | 12; 12; 12; 6; 6; 6; 12; 12; 12; 6; 6; 6; 12; 6; 8; 8; 12; 12; 12; 6 |
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; [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 | ASARUM CANADENSE ROOT; BLATTA ORIENTALIS; BUFO BUFO CUTANEOUS GLAND; CLEMATIS RECTA FLOWERING TOP; CUPRIC ACETATE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; SODIUM CHLORIDE; SODIUM |
Labeler Name | Deseret Biologicals, Inc. |
Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Insect Allergenic Extract [EPC] |
DEA Schedule | n/a |
Marketing Category | UNAPPROVED HOMEOPATHIC |
Application Number | n/a |
Listing Certified Through | 2024-12-31 |
Package
NDC 43742-2089-01 (43742208901)
NDC Package Code | 43742-2089-1 |
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Billing NDC | 43742208901 |
Package | 30 mL in 1 BOTTLE, DROPPER (43742-2089-1) |
Marketing Start Date | 2023-08-23 |
NDC Exclude Flag | N |
Pricing Information | N/A |