FCS HP

Product NDC
43406-0696
11-digit product format
434060696
Labeler code
43406
Product ID
43406-0696_52f33d9b-a7a3-469e-8c8c-841d6655ab7f
Type
HUMAN OTC DRUG
Nonproprietary name
Epinephrine,GlutamicAcid,MucunaPruriensSeed,Niacinamide,Serotonin,Ubidecarenone,Corticotropin,AdenosineTriphosphate,InsulinPork,SusScrofaParathyroidGland,SusScrofaPituitaryGland,ThiamineHydrochloride,Thyroid,AnhydrousCitricAcid,HerringSpermDNA,SaccharomycesCerevisiaeRNA,AnacardiumOccidentaleFruit,ArsenicTrioxide,AsparticAcid,BariumCarbonate,OysterShellCalciumCarbonateCrude,ClematisRectaFloweringTop,LycopodiumClavatumSpore,AnemonePulsatilla,DaturaStramonium,Sulfur
Dosage form
LIQUID
Route
ORAL
Labeler
Natural Creations, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2018-06-01
Substance
EPINEPHRINE; GLUTAMIC ACID; MUCUNA PRURIENS SEED; NIACINAMIDE; SEROTONIN; UBIDECARENONE; CORTICOTROPIN; ADENOSINE TRIPHOSPHATE; INSULIN PORK; SUS SCROFA PARATHYROID GLAND; SUS SCROFA PITUITARY GLAND; THIAMINE HYDROCHLORIDE; THYROID, UNSPECIFIED; ANHYDROUS CITRIC ACID; HERRING SPERM DNA; SACCHAROMYCES CEREVISIAE RNA; ANACARDIUM OCCIDENTALE FRUIT; ARSENIC TRIOXIDE; ASPARTIC ACID; BARIUM CARBONATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CLEMATIS RECTA FLOWERING TOP; LYCOPODIUM CLAVATUM SPORE; ANEMONE PULSATILLA; DATURA STRAMONIUM; SULFUR
Active strength
30; 30; 30; 9; 30; 9; 30; 6; 6; 6; 6; 6; 6; 12; 12; 12; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/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; [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; [hp_C]/mL
Pharmacologic classes
Acidifying Activity [MoA], Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Catecholamine [EPC], Catecholamines [CS], Decreased Coagulation Factor Activity [PE], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
FCS HP
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EPINEPHRINE30 [hp_C]/mL
GLUTAMIC ACID30 [hp_C]/mL
MUCUNA PRURIENS SEED30 [hp_C]/mL
NIACINAMIDE9 [hp_X]/mL
SEROTONIN30 [hp_C]/mL
UBIDECARENONE9 [hp_X]/mL
CORTICOTROPIN30 [hp_C]/mL
ADENOSINE TRIPHOSPHATE6 [hp_C]/mL
INSULIN PORK6 [hp_C]/mL
SUS SCROFA PARATHYROID GLAND6 [hp_C]/mL
SUS SCROFA PITUITARY GLAND6 [hp_C]/mL
THIAMINE HYDROCHLORIDE6 [hp_C]/mL
THYROID, UNSPECIFIED6 [hp_C]/mL
ANHYDROUS CITRIC ACID12 [hp_C]/mL
HERRING SPERM DNA12 [hp_C]/mL
SACCHAROMYCES CEREVISIAE RNA12 [hp_C]/mL
ANACARDIUM OCCIDENTALE FRUIT30 [hp_C]/mL
ARSENIC TRIOXIDE30 [hp_C]/mL
ASPARTIC ACID30 [hp_C]/mL
BARIUM CARBONATE30 [hp_C]/mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE30 [hp_C]/mL
CLEMATIS RECTA FLOWERING TOP30 [hp_C]/mL
LYCOPODIUM CLAVATUM SPORE30 [hp_C]/mL
ANEMONE PULSATILLA30 [hp_C]/mL
DATURA STRAMONIUM30 [hp_C]/mL
SULFUR30 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 2 · 26 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
YKH834O4BHInternal UNII lookup
3KX376GY7LInternal UNII lookup
55G8SQ543SInternal UNII lookup
25X51I8RD4Internal UNII lookup
333DO1RDJYInternal UNII lookup
EJ27X76M46Internal UNII lookup
K0U68Q2TXAInternal UNII lookup
8L70Q75FXEInternal UNII lookup
AVT680JB39Internal UNII lookup
2KBE35NE8SInternal UNII lookup
L0PFEMQ1DTInternal UNII lookup
M572600E5PInternal UNII lookup
0B4FDL9I6PInternal UNII lookup
XF417D3PSLInternal UNII lookup
51FI676N6FInternal UNII lookup
J17GBZ5VGXInternal UNII lookup
4A10JR4E7EInternal UNII lookup
S7V92P67HOInternal UNII lookup
30KYC7MIAIInternal UNII lookup
6P669D8HQ8Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
ba8fed68-f27f-4651-adec-0994a5375887Available 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
cf050ccd-1144-f76a-e00d-e5698d8597d4Product name620250625
b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
7314d8f7-fa99-4dc2-9f68-de2ff142f4b7Product name220250121
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
e0031c74-3853-42bc-8e10-86dbbe83992eProduct name220231116
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
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
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0696-12021-11-12C16284748780-1ba0f9c33-5105-a910-e053-dadaa90a0b85FCS HP
43406-0696-12021-01-29C16284748780-1ba0f9c33-5105-a910-e053-dadaa90a0b85FCS HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0696-1FCS HP30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43406-0696FCS HP (EPINEPHRINE,GLUTAMICACID,MUCUNAPRURIENSSEED,NIACINAMIDE,SEROTONIN,UBIDECARENONE,CORTICOTROPIN,ADENOSINETRIPHOSPHATE,INSULINPORK,SUSSCROFAPARATHYROIDGLAND,SUSSCROFAPITUITARYGLAND,THIAMINEHYDROCHLORIDE,THYROID,ANHYDROUSCITRICACID,HERRINGSPERMDNA,SACCHAROMYCESCEREVISIAERNA,ANACARDIUMOCCIDENTALEFRUIT,ARSENICTRIOXIDE,ASPARTICACID,BARIUMCARBONATE,OYSTERSHELLCALCIUMCARBONATECRUDE,CLEMATISRECTAFLOWERINGTOP,LYCOPODIUMCLAVATUMSPORE,ANEMONEPULSATILLA,DATURASTRAMONIUM,SULFUR) LIQUID [NATURAL CREATIONS, INC.]2Current NDC, Legacy NDC, 1 package rows20211113_ba8fed68-f27f-4651-adec-0994a5375887.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
FCS HPEPINEPHRINE,GLUTAMICACID,MUCUNAPRURIENSSEED,NIACINAMIDE,SEROTONIN,UBIDECARENONE,CORTICOTROPIN,ADENOSINETRIPHOSPHATE,INSULINPORK,SUSSCROFAPARATHYROIDGLAND,SUSSCROFAPITUITARYGLAND,THIAMINEHYDROCHLORIDE,THYROID,ANHYDROUSCITRICACID,HERRINGSPERMDNA,SACCHAROMYCESCEREVISIAERNA,ANACARDIUMOCCIDENTALEFRUIT,ARSENICTRIOXIDE,ASPARTICACID,BARIUMCARBONATE,OYSTERSHELLCALCIUMCARBONATECRUDE,CLEMATISRECTAFLOWERINGTOP,LYCOPODIUMCLAVATUMSPORE,ANEMONEPULSATILLA,DATURASTRAMONIUM,SULFURNatural Creations, Inc.ba8fed68-f27f-4651-adec-0994a53758872025-12-10WarningsExact identifier
ndc (product): 43406-0696

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43406-0696-14340606960130 mL in 1 BOTTLE, DROPPER (43406-0696-1) 30 ml2018-06-010000-00-00NoNoCurrent