FDA.reportPublic FDA data

Adrenapath

Manufacturer
Energetix Corporation
Effective date
2026-08-11
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
daily-update
Hydrated at
2026-08-13 01:00:59

Label at a glance#

ProductAdrenapath
Active ingredientMILK THISTLE, CHELIDONIUM MAJUS, ECHINACEA ANGUSTIFOLIA, SUS SCROFA ADRENAL GLAND, SODIUM CHLORIDE, PHOSPHORIC ACID, BOS TAURUS PITUITARY GLAND, THYROID, BOVINE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

​Active ingredients​​

59.1 mL contains 7.69% of Carduus mar 12X; Chelidonium maj 4X; Echinacea 4X; Glandula suprarenalis suis 9X, 12X, 6C; Nat mur 12X; Phosphoricum ac 12X; Pituitarum posterium 12X, 6C; Thyroidinum 9X, 12X, 6C.

Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS & USAGE SECTION

​Uses​​

Temporary relief of exhaustion, cravings, restless sleep.

WARNINGS SECTION

​Warnings

  • In case of overdose, get medical help or contact a Poison Control Center right away.
  • If pregnant or breast-feeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

​Directions

  • Take 30 drops orally twice daily or as directed by a healthcare professional.
  • Consult a physician for use in children under 12 years of age or if symptoms worsen or persist.

OTHER SAFETY INFORMATION

​Other information

  • Store at room temperature out of direct sunlight.
  • Do not use if neck wrap is broken or missing.
  • Shake well before use.

INACTIVE INGREDIENT SECTION

​Inactive ingredients

Cane Alcohol, Vegetable Glycerin, Purified Water.

OTC - QUESTIONS SECTION

Distributed by Energetix Corp.

Dahlonega, GA 30533

Questions? Comments?

800.990.7085

www.energetix.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

energetix

Adrenapath

Homeopathic Remedy

Exhaustion, cravings, restless sleep

2 fl oz (59.1 mL) / 15% Cane Alcohol

Adrenapath r09-25 04011Adrenapath r09-25 04011

OTC - PURPOSE SECTION

Purpose Temporary relief of exhaustion, cravings, restless sleep.

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64578-0096-12021-12-15C16284748780-1ba0f9c33-568a-a910-e053-dadaa90a0b85Adrenapath ​
64578-0096-12021-12-15C16284748780-1ba0f9c33-568a-a910-e053-dadaa90a0b85Adrenapath ​
64578-0096-12021-01-29C16284748780-1ba0f9c33-568a-a910-e053-dadaa90a0b85Adrenapath ​
64578-0096-12021-01-29C16284748780-1ba0f9c33-568a-a910-e053-dadaa90a0b85Adrenapath ​

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNN1
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US81
MILK THISTLEACTIVE INGREDIENTU946SH95EE1
PHOSPHORIC ACIDACTIVE INGREDIENTE4GA8884NN1
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
SUS SCROFA ADRENAL GLANDACTIVE INGREDIENT398IYQ16YV1
SUS SCROFA PITUITARY GLANDACTIVE INGREDIENTE8S87O660T1
THYROID, UNSPECIFIEDACTIVE INGREDIENT0B4FDL9I6P1
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNN1
CHLORIDE IONACTIVE MOIETYQ32ZN486981
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US81
MILK THISTLEACTIVE MOIETYU946SH95EE1
PHOSPHORIC ACIDACTIVE MOIETYE4GA8884NN1
SUS SCROFA ADRENAL GLANDACTIVE MOIETY398IYQ16YV1
SUS SCROFA PITUITARY GLANDACTIVE MOIETYE8S87O660T1
THYROID, UNSPECIFIEDACTIVE MOIETY0B4FDL9I6P1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64578-009664578-0096-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
MILK THISTLEU946SH95EEACTIB
CHELIDONIUM MAJUS7E889U5RNNACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
BOS TAURUS PITUITARY GLAND7JM57I419KACTIB
THYROID, BOVINEMN18OTN73WACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
112025-07-11full-release2026-06-01 02:34:27

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
AdrenapathCARDUUS MARIANUS, CHELIDONIUM MAJUS, ECHINACEA (ANGUSTIFOLIA), GLANDULA SUPRARENALIS SUIS, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PITUITARUM POSTERIUM (BOVINE), THYROIDINUM (BOVINE)Energetix Corporationc300b8f5-4334-4597-a303-8200cbc117d12026-08-11WarningsExact identifier
ndc (package): 64578-0096-1
ndc (product): 64578-0096
ndc11 (package): 64578009601
spl id: 58c87689-8864-6e2f-e063-6294a90a9ac3
spl set id: c300b8f5-4334-4597-a303-8200cbc117d1

Reported adverse events (FAERS/openFDA)#

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