warnings
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. Keep out of reach of children.
ReHydration
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- ReHydration
- Generic name
- ADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS, KALI PHOS, NAT MUR, SARSAPARILLA, SILICEA, TARAXACUM, THYROIDINUM
- Manufacturer
- Energetix Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 37063a49-6b45-4167-875d-49c9dac3f79b
- SPL ID
- 275c7a3b-21d1-eaed-e063-6394a90a44ab
- Version
- 3
- Effective date
- 2024-11-20
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:19
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | ReHydration | openfda.brand_name | |
| generic name | ADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS, KALI PHOS, NAT MUR, SARSAPARILLA, SILICEA, TARAXACUM, THYROIDINUM | openfda.generic_name | |
| manufacturer name | Energetix Corporation | openfda.manufacturer_name | |
| ndc | package | 64578-0177-1 | openfda.package_ndc |
| ndc | product | 64578-0177 | openfda.product_ndc |
| ndc11 | package | 64578017701 | derived:openfda.package_ndc |
| spl id | 275c7a3b-21d1-eaed-e063-6394a90a44ab | id | |
| spl set id | 37063a49-6b45-4167-875d-49c9dac3f79b | set_id | |
| unii | CI71S98N1Z | openfda.unii | |
| unii | 3SW678MX72 | openfda.unii | |
| unii | 0B4FDL9I6P | openfda.unii | |
| unii | 2H1576D5WG | openfda.unii | |
| unii | 39981FM375 | openfda.unii | |
| unii | ETJ7Z6XBU4 | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | S6G2NLH4Y7 | openfda.unii | |
| unii | 398IYQ16YV | openfda.unii | |
| unii | E0399OZS9N | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.