Panacode

Product NDC
43406-0686
11-digit product format
434060686
Labeler code
43406
Product ID
43406-0686_c01cadca-563b-4895-be5d-19be32a38f03
Type
HUMAN OTC DRUG
Nonproprietary name
Syzygium, Hydrastis, Adrenalinum, Pancreatinum, Pituitarum Posterium, Bovista, Insulin, Lycopersicum, Phosphoricum Ac, Phosphorus, Tarentula Hispana, Terebinthina, Uranium Nitricum
Dosage form
LIQUID
Route
ORAL
Labeler
Natural Creations, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-02-11
Substance
EPINEPHRINE; GOLDENSEAL; INSULIN PORK; LYCOPERDON UTRIFORME FRUITING BODY; LYCOSA TARANTULA; PANCRELIPASE; PHOSPHORIC ACID; PHOSPHORUS; SOLANUM LYCOPERSICUM WHOLE; SUS SCROFA PITUITARY GLAND, POSTERIOR; SYZYGIUM CUMINI SEED; TURPENTINE OIL; URANYL NITRATE HEXAHYDRATE
Active strength
9; 6; 12; 12; 12; 9; 12; 12; 12; 9; 4; 12; 12 [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
Pharmacologic classes
Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], 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
Panacode
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SYZYGIUM CUMINI SEED9 [hp_X]/mL
GOLDENSEAL6 [hp_X]/mL
EPINEPHRINE12 [hp_X]/mL
PANCRELIPASE12 [hp_X]/mL
SUS SCROFA PITUITARY GLAND, POSTERIOR12 [hp_X]/mL
LYCOPERDON UTRIFORME FRUITING BODY9 [hp_X]/mL
INSULIN PORK12 [hp_X]/mL
SOLANUM LYCOPERSICUM WHOLE12 [hp_X]/mL
PHOSPHORIC ACID12 [hp_X]/mL
PHOSPHORUS9 [hp_X]/mL
LYCOSA TARANTULA4 [hp_X]/mL
TURPENTINE OIL12 [hp_X]/mL
URANYL NITRATE HEXAHYDRATE12 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 13 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
820LSF646IInternal UNII lookup
ZW3Z11D0JVInternal UNII lookup
YKH834O4BHInternal UNII lookup
FQ3DRG0N5KInternal UNII lookup
E8S87O660TInternal UNII lookup
K2A74U428FInternal UNII lookup
AVT680JB39Internal UNII lookup
0243Q4990LInternal UNII lookup
E4GA8884NNInternal UNII lookup
27YLU75U4WInternal UNII lookup
86M454L2TTInternal UNII lookup
C5H0QJ6V7FInternal UNII lookup
3V057702FYInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
f2144c14-28a2-4dc4-b517-0f81e9c8b720Available 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
49628fc7-2031-4c28-bd31-0ef3aa8f44a3Product name320251118
cbf85893-59ef-423f-87d4-a573c000a8b9Product name820250731
b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
e0031c74-3853-42bc-8e10-86dbbe83992eProduct name220231116
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
0b1603b8-969e-b082-f6f5-ad66d8a6ea8aProduct name220200325
19041f15-771b-3d3a-88fc-f5e2d079cd6dProduct name220200325
1987d950-08e4-4b70-adeb-fb67a71142abProduct name220200325
8825ddf7-1520-4680-b0ee-684e2fa73672Product name220200325
2686d634-e712-4007-8dbf-3d37c6c4d71fProduct name120181121
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
bd49bb86-2d32-4a7a-a594-eeda2e29af42Product name120180118
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
3becbe78-12d9-4ad2-9b4c-1e36f8d1303aProduct name120170815
267a6f34-90b4-2f48-3063-4f505d06a7beProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0686-1Panacode30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0686PANACODE (SYZYGIUM, HYDRASTIS, ADRENALINUM, PANCREATINUM, PITUITARUM POSTERIUM, BOVISTA, INSULIN, LYCOPERSICUM, PHOSPHORICUM AC, PHOSPHORUS, TARENTULA HISPANA, TEREBINTHINA, URANIUM NITRICUM) LIQUID [NATURAL CREATIONS, INC]1Current NDC, Legacy NDC, 1 package rows20230111_f2144c14-28a2-4dc4-b517-0f81e9c8b720.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
PanacodeSYZYGIUM, HYDRASTIS, ADRENALINUM, PANCREATINUM, PITUITARUM POSTERIUM, BOVISTA, INSULIN, LYCOPERSICUM, PHOSPHORICUM AC, PHOSPHORUS, TARENTULA HISPANA, TEREBINTHINA, URANIUM NITRICUMNatural Creations, Incf2144c14-28a2-4dc4-b517-0f81e9c8b7202025-12-16WarningsExact identifier
ndc (product): 43406-0686

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43406-0686-14340606860130 mL in 1 BOTTLE, DROPPER (43406-0686-1) 30 ml2020-02-110000-00-00NoNoCurrent