Erogetone

Product NDC
44911-0552
11-digit product format
449110552
Labeler code
44911
Product ID
44911-0552_ac359f38-feb3-49b4-b9b0-6a291ec67aa6
Type
HUMAN OTC DRUG
Nonproprietary name
Aralia Quinquefolia, Berberis Vulgaris, Causticum, Conium Maculatum, Damiana, Graphites, Lachesis Mutus, Natrum Muriaticum, Phosphoricum Acidum, Phosphorus, Sepia
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-10-06
Marketing end
2026-10-26
Substance
AMERICAN GINSENG; BERBERIS VULGARIS ROOT BARK; CAUSTICUM; CONIUM MACULATUM FLOWERING TOP; GRAPHITE; LACHESIS MUTA VENOM; PHOSPHORIC ACID; PHOSPHORUS; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; TURNERA DIFFUSA LEAFY TWIG
Active strength
3; 3; 12; 12; 12; 12; 12; 12; 12; 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
NDC exclude flag
No
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Erogetone

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMERICAN GINSENG3 [hp_X]/mL
BERBERIS VULGARIS ROOT BARK3 [hp_X]/mL
CAUSTICUM12 [hp_X]/mL
CONIUM MACULATUM FLOWERING TOP12 [hp_X]/mL
TURNERA DIFFUSA LEAFY TWIG12 [hp_X]/mL
GRAPHITE12 [hp_X]/mL
LACHESIS MUTA VENOM12 [hp_X]/mL
SODIUM CHLORIDE12 [hp_X]/mL
PHOSPHORIC ACID12 [hp_X]/mL
PHOSPHORUS12 [hp_X]/mL
SEPIA OFFICINALIS JUICE12 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 11 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8W75VCV53QInternal UNII lookup
1TH8Q20J0UInternal UNII lookup
DD5FO1WKFUInternal UNII lookup
Q28R5GF371Internal UNII lookup
RQ2CFA7WWJInternal UNII lookup
4QQN74LH4OInternal UNII lookup
VSW71SS07IInternal UNII lookup
451W47IQ8XInternal UNII lookup
E4GA8884NNInternal UNII lookup
27YLU75U4WInternal UNII lookup
QDL83WN8C2Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
1e872ecd-e7a5-463d-9832-47b7046096dbAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0552-1Erogetone30 mL in 1 BOTTLE, DROPPERLIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0552EROGETONE (ARALIA QUINQUEFOLIA, BERBERIS VULGARIS, CAUSTICUM, CONIUM MACULATUM, DAMIANA, GRAPHITES, LACHESIS MUTUS, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SEPIA) LIQUID [ENERGIQUE, INC.]3Current NDC, Legacy NDC, 1 package rows20220630_1e872ecd-e7a5-463d-9832-47b7046096db.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
ErogetoneARALIA QUINQUEFOLIA, BERBERIS VULGARIS, CAUSTICUM, CONIUM MACULATUM, DAMIANA, GRAPHITES, LACHESIS MUTUS, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SEPIAEnergique, Inc.1e872ecd-e7a5-463d-9832-47b7046096db2022-06-28WarningsExact identifier
ndc (product): 44911-0552

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0552-14491105520130 mL in 1 BOTTLE, DROPPER (44911-0552-1) 30 ml2020-10-062026-10-26NoNoCurrent