FDA.reportPublic FDA data

ReHydration

Manufacturer
Energetix Corp | Apotheca Company
Effective date
2017-01-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:08:33

Label at a glance#

ProductReHydration
Active ingredientADENOSINE CYCLIC PHOSPHATE, ARABICA COFFEE BEAN, SUS SCROFA ADRENAL GLAND, BOS TAURUS HYPOTHALAMUS, POTASSIUM PHOSPHATE, DIBASIC, SODIUM CHLORIDE, SARSAPARILLA, SILICON DIOXIDE, TARAXACUM OFFICINALE, THYROID, BOVINE
Label structure9 sections

Indications and uses

Temporary relief of increased or decreased thirst, dryness, headaches, low energy, mental sluggishness.

Dosage and administration

MUST BE ADDED TO LIQUID. Add 15 drops per liter of water or as directed by a healthcare professional. Shake well before use. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Adenosinum Cyclophosphoricum 12X, 30X; Coffea Cruda 9X; Glandula Suprarenalis Suis 9X, 12X ,6C; Hypothalamus (Bovine) 12X, 6C, 12C; Kali Phosphoricum 6X, 12X, 30X; Natrum Muriaticum 8X, 12X, 30X; Sarsaparilla 4X, 6X, 12X, 6C; Silicea 12X, 30X; Taraxacum Officinale 4X; Thyroidinum (Bovine) 12X, 6C, 12C.

PURPOSE:

OTC - PURPOSE SECTION

Temporary relief of increased or decreased thirst, dryness, headaches, low energy, mental sluggishness.

WARNINGS:

WARNINGS SECTION

In case of overdose, get medical help or call a Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.


Other Information

Store in cool, dry place out of direct sunlight.

Do not use if neck wrap is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

MUST BE ADDED TO LIQUID. Add 15 drops per liter of water or as directed by a healthcare professional.

Shake well before use.

Consult a physician for use in children under 12 years of age.

USES:

INDICATIONS & USAGE SECTION

Temporary relief of increased or decreased thirst, dryness, headaches, low energy, mental sluggishness.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Ethyl Alcohol, Glycerin, Purified Water.

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by
Energetix Corp
Dahlonega, GA 30533
Questions? Comments?
800.990.7085
www.goenergetix.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

energetix

ReHydration

Homeopathic Remedy

Increased or decreased thirst, dryness,
headaches, low energy, mental sluggishness.

2 fl oz (59.1 mL)

ReHydrationReHydration

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
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
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
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
64578-0090-2ReHydration59.1 mL in 1 BOTTLE, DROPPERLIQUID59.15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64578-0090REHYDRATION (ADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI PHOSPHORICUM, NATRUM MURIATICUM, SARSAPARILLA, SILICEA, TARAXACUM OFFICINALE, THYROIDINUM (BOVINE)) LIQUID [ENERGETIX CORP]5Current NDC, Legacy NDC, 1 package rows20170214_9883c502-9782-451e-9eec-c54d7b054f31.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ADENOSINE CYCLIC PHOSPHATEACTIVE INGREDIENTE0399OZS9N2
ARABICA COFFEE BEANACTIVE INGREDIENT3SW678MX722
BOS TAURUS HYPOTHALAMUSACTIVE INGREDIENTS6G2NLH4Y72
POTASSIUM PHOSPHATE, DIBASICACTIVE INGREDIENTCI71S98N1Z2
SARSAPARILLAACTIVE INGREDIENT2H1576D5WG2
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU42
SODIUM SULFATEACTIVE INGREDIENT0YPR65R21J2
SUS SCROFA ADRENAL GLANDACTIVE INGREDIENT398IYQ16YV2
TARAXACUM OFFICINALEACTIVE INGREDIENT39981FM3752
THYROID, UNSPECIFIEDACTIVE INGREDIENT0B4FDL9I6P2
ADENOSINE CYCLIC 3',5'-PHOSPHATEACTIVE MOIETYE0399OZS9N2
ARABICA COFFEE BEANACTIVE MOIETY3SW678MX722
BOS TAURUS HYPOTHALAMUSACTIVE MOIETYS6G2NLH4Y72
COLLOIDAL SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU42
PHOSPHATE IONACTIVE MOIETYNK08V8K8HR2
SARSAPARILLAACTIVE MOIETY2H1576D5WG2
SODIUM SULFATE ANHYDROUSACTIVE MOIETY36KCS0R7502
SUS SCROFA ADRENAL GLANDACTIVE MOIETY398IYQ16YV2
TARAXACUM OFFICINALEACTIVE MOIETY39981FM3752
THYROID, UNSPECIFIEDACTIVE MOIETY0B4FDL9I6P2
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
GLYCERININACTIVE INGREDIENTPDC6A3C0OX2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64578-009064578-0090-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ADENOSINE CYCLIC PHOSPHATEE0399OZS9NACTIB
ARABICA COFFEE BEAN3SW678MX72ACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
BOS TAURUS HYPOTHALAMUSS6G2NLH4Y7ACTIB
POTASSIUM PHOSPHATE, DIBASICCI71S98N1ZACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
SARSAPARILLA2H1576D5WGACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
TARAXACUM OFFICINALE39981FM375ACTIB
THYROID, BOVINEMN18OTN73WACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

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
GLYCERINGLYCERINPDC6A3C0OXLIQUID / ORAL2400 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
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 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
ReHydrationADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI PHOSPHORICUM, NATRUM MURIATICUM, SARSAPARILLA, SILICEA, TARAXACUM OFFICINALE, THYROIDINUM (BOVINE)Energetix Corp9883c502-9782-451e-9eec-c54d7b054f312017-01-31WarningsExact identifier
ndc (package): 64578-0090-2
ndc (product): 64578-0090
ndc11 (package): 64578009002
spl id: 8f74c592-87fa-42b0-968b-fd0260e4c9b0
spl set id: 9883c502-9782-451e-9eec-c54d7b054f31

Reported adverse events (FAERS/openFDA)#

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