ReHydration

Product NDC
64578-0177
Requested package NDC
64578-0177-1
11-digit product format
645780177
Labeler code
64578
Product ID
64578-0177_275c7a3b-21d1-eaed-e063-6394a90a44ab
Type
HUMAN OTC DRUG
Nonproprietary name
Adenosinum cyclophosphoricum, Coffea cruda, Glandula suprarenalis suis, Hypothalamus, Kali phos, Nat mur, Sarsaparilla, Silicea, Taraxacum, Thyroidinum
Dosage form
LIQUID
Route
ORAL
Labeler
Energetix Corporation
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-04-12
Substance
ADENOSINE CYCLIC PHOSPHATE; ARABICA COFFEE BEAN; SUS SCROFA ADRENAL GLAND; BOS TAURUS HYPOTHALAMUS; DIBASIC POTASSIUM PHOSPHATE; SODIUM CHLORIDE; SILICON DIOXIDE; SMILAX ORNATA ROOT; TARAXACUM OFFICINALE; THYROID, UNSPECIFIED
Active strength
12; 9; 9; 12; 6; 8; 12; 4; 4; 12 [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], 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
ReHydration
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ADENOSINE CYCLIC PHOSPHATE12 [hp_X]/59.1mL
ARABICA COFFEE BEAN9 [hp_X]/59.1mL
SUS SCROFA ADRENAL GLAND9 [hp_X]/59.1mL
BOS TAURUS HYPOTHALAMUS12 [hp_X]/59.1mL
DIBASIC POTASSIUM PHOSPHATE6 [hp_X]/59.1mL
SODIUM CHLORIDE8 [hp_X]/59.1mL
SILICON DIOXIDE12 [hp_X]/59.1mL
SMILAX ORNATA ROOT4 [hp_X]/59.1mL
TARAXACUM OFFICINALE4 [hp_X]/59.1mL
THYROID, UNSPECIFIED12 [hp_X]/59.1mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 10 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
E0399OZS9NInternal UNII lookup
3SW678MX72Internal UNII lookup
398IYQ16YVInternal UNII lookup
S6G2NLH4Y7Internal UNII lookup
CI71S98N1ZInternal UNII lookup
451W47IQ8XInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
2H1576D5WGInternal UNII lookup
39981FM375Internal UNII lookup
0B4FDL9I6PInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
37063a49-6b45-4167-875d-49c9dac3f79bAvailable on FDA.report

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
64578-0177-1ReHydration59.1 mL in 1 BOTTLELIQUID59.13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64578-0177REHYDRATION (ADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS, KALI PHOS, NAT MUR, SARSAPARILLA, SILICEA, TARAXACUM, THYROIDINUM) LIQUID [ENERGETIX CORP]2Current NDC, 1 package rows20231230_37063a49-6b45-4167-875d-49c9dac3f79b.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
ReHydrationADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS, KALI PHOS, NAT MUR, SARSAPARILLA, SILICEA, TARAXACUM, THYROIDINUMEnergetix Corporation37063a49-6b45-4167-875d-49c9dac3f79b2024-11-20WarningsExact identifier
ndc (package): 64578-0177-1
ndc (product): 64578-0177
ndc11 (package): 64578017701

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
64578-0177-16457801770159.1 mL in 1 BOTTLE (64578-0177-1) 59.1 ml2023-04-12NoNoCurrent