Homeoplex G

Product NDC
71781-0005
11-digit product format
717810005
Labeler code
71781
Product ID
71781-0005_1c6495b2-b51b-4b59-866c-f7dd2feee6db
Type
HUMAN OTC DRUG
Nonproprietary name
Gentiana Lutea, Arsenicum Album, Cinchona Officinalis, Colocynthis, Nux Vomica, Phosphorus, Small Intestine (Suis)
Dosage form
LIQUID
Route
ORAL
Labeler
Supplement Clinic, LLC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-11-01
Substance
GENTIANA LUTEA ROOT; ARSENIC TRIOXIDE; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; PORK INTESTINE
Active strength
3; 12; 12; 12; 12; 12; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
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
Homeoplex G
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GENTIANA LUTEA ROOT3 [hp_X]/mL
ARSENIC TRIOXIDE12 [hp_X]/mL
CINCHONA OFFICINALIS BARK12 [hp_X]/mL
CITRULLUS COLOCYNTHIS FRUIT PULP12 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED12 [hp_X]/mL
PHOSPHORUS12 [hp_X]/mL
PORK INTESTINE30 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 7 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
S72O3284MSInternal UNII lookup
S7V92P67HOInternal UNII lookup
S003A158SBInternal UNII lookup
23H32AOH17Internal UNII lookup
269XH13919Internal UNII lookup
27YLU75U4WInternal UNII lookup
40GMI0R60LInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4119921d-6c71-41ab-98b6-b86c820eb8bcAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71781-0005-1Homeoplex G60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71781-0005HOMEOPLEX G (GENTIANA LUTEA, ARSENICUM ALBUM, CINCHONA OFFICINALIS, COLOCYNTHIS, NUX VOMICA, PHOSPHORUS, SMALL INTESTINE (SUIS)) LIQUID [SUPPLEMENT CLINIC, LLC.]1Current NDC, Legacy NDC, 1 package rows20171102_4119921d-6c71-41ab-98b6-b86c820eb8bc.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
Homeoplex GGENTIANA LUTEA, ARSENICUM ALBUM, CINCHONA OFFICINALIS, COLOCYNTHIS, NUX VOMICA, PHOSPHORUS, SMALL INTESTINE (SUIS)Supplement Clinic, LLC.4119921d-6c71-41ab-98b6-b86c820eb8bc2017-11-01WarningsExact identifier
ndc (product): 71781-0005

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71781-0005-17178100050160 mL in 1 BOTTLE, DROPPER (71781-0005-1) 60 ml2017-11-010000-00-00NoNoCurrent