Bio Mood Phase

Product NDC
43742-1258
11-digit product format
437421258
Labeler code
43742
Product ID
43742-1258_d75fc007-3071-4114-9cb5-4aa4686778a3
Type
HUMAN OTC DRUG
Nonproprietary name
Cortisone Aceticum, Adrenalinum, Chininum Arsenicosum, Helonias Dioica, Hypericum Perforatum, Kali Phosphoricum, Nux Vomica, Selenium Metallicum, Aurum Metallicum, Bacillus 7 (Enterobacter Cloacae)
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-09-11
Substance
CHAMAELIRIUM LUTEUM ROOT; CORTISONE ACETATE; DIBASIC POTASSIUM PHOSPHATE; ENTEROBACTER CLOACAE; EPINEPHRINE; GOLD; HYPERICUM PERFORATUM WHOLE; QUININE ARSENATE; SELENIUM; STRYCHNOS NUX-VOMICA SEED
Active strength
10; 8; 10; 30; 8; 10; 10; 10; 10; 10 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Allergens [CS], Antimalarial [EPC], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Chemical Allergen [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Bio Mood Phase
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CORTISONE ACETATE10 [hp_C]/mL
EPINEPHRINE8 [hp_C]/mL
QUININE ARSENATE10 [hp_C]/mL
CHAMAELIRIUM LUTEUM ROOT30 [hp_C]/mL
HYPERICUM PERFORATUM WHOLE8 [hp_C]/mL
DIBASIC POTASSIUM PHOSPHATE10 [hp_C]/mL
STRYCHNOS NUX-VOMICA SEED10 [hp_C]/mL
SELENIUM10 [hp_C]/mL
GOLD10 [hp_C]/mL
ENTEROBACTER CLOACAE10 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
883WKN7W8XInternal UNII lookup
YKH834O4BHInternal UNII lookup
8C15XFK30PInternal UNII lookup
DQV54Y5H3UInternal UNII lookup
XK4IUX8MNBInternal UNII lookup
CI71S98N1ZInternal UNII lookup
269XH13919Internal UNII lookup
H6241UJ22BInternal UNII lookup
79Y1949PYOInternal UNII lookup
40OMQ8YEPDInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
81d6e6db-94dc-4b6f-9ef7-9180ec54eebfAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0b4ec9ca-d305-43fc-88dd-7a510313efe0Product name120260105
bb209f42-a85f-4fee-9d3d-c9dded168625Product name120251208
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
49628fc7-2031-4c28-bd31-0ef3aa8f44a3Product name320251118
cbf85893-59ef-423f-87d4-a573c000a8b9Product name820250731
b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
e0031c74-3853-42bc-8e10-86dbbe83992eProduct name220231116
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
2686d634-e712-4007-8dbf-3d37c6c4d71fProduct name120181121
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
bd49bb86-2d32-4a7a-a594-eeda2e29af42Product name120180118
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
3becbe78-12d9-4ad2-9b4c-1e36f8d1303aProduct name120170815
22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
9bfd9c37-f773-6e9a-5f6b-6f5701d62adcProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43742-1258-1Bio Mood Phase30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1258BIO MOOD PHASE (CORTISONE ACETICUM, ADRENALINUM, CHININUM ARSENICOSUM, HELONIAS DIOICA, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, NUX VOMICA, SELENIUM METALLICUM, AURUM METALLICUM, BACILLUS 7 (ENTEROBACTER CLOACAE)) LIQUID [DESERET BIOLOGICALS, INC.]2Current NDC, Legacy NDC, 1 package rows20240427_81d6e6db-94dc-4b6f-9ef7-9180ec54eebf.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bio Mood PhaseCORTISONE ACETICUM, ADRENALINUM, CHININUM ARSENICOSUM, HELONIAS DIOICA, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, NUX VOMICA, SELENIUM METALLICUM, AURUM METALLICUM, BACILLUS 7 (ENTEROBACTER CLOACAE)Deseret Biologicals, Inc.81d6e6db-94dc-4b6f-9ef7-9180ec54eebf2024-04-26WarningsExact identifier
ndc (product): 43742-1258

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1258-14374212580130 mL in 1 BOTTLE, DROPPER (43742-1258-1) 30 ml2018-09-110000-00-00NoNoCurrent