warnings
Warnings In case of overdose, get medical help or contact a Poison Control Center right away. If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. Keep out of reach of children
Endopath-F
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
- Endopath-F
- Generic name
- AGNUS, ANGELICA SIN, CIMICIFUGA, FUCUS, GLANDULA SUPRARENALIS SUIS, GLYCYRRHIZA, HYPOTHALAMUS, OOPHORINUM, PITUITARUM POSTERIUM, PULSATILLA, SEPIA, THYROIDINUM, XANTHOXYLUM
- Manufacturer
- Energetix Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d0880c30-54f5-4af4-ad5d-85ecae3bb9e5
- SPL ID
- 2903c621-c6e2-9048-e063-6394a90a7fa6
- Version
- 4
- Effective date
- 2025-07-15
- Source export date
- 2026-10-12
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:44:49
| 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 | Endopath-F | openfda.brand_name | |
| generic name | AGNUS, ANGELICA SIN, CIMICIFUGA, FUCUS, GLANDULA SUPRARENALIS SUIS, GLYCYRRHIZA, HYPOTHALAMUS, OOPHORINUM, PITUITARUM POSTERIUM, PULSATILLA, SEPIA, THYROIDINUM, XANTHOXYLUM | openfda.generic_name | |
| manufacturer name | Energetix Corporation | openfda.manufacturer_name | |
| ndc | package | 64578-0170-1 | openfda.package_ndc |
| ndc | product | 64578-0170 | openfda.product_ndc |
| ndc11 | package | 64578017001 | derived:openfda.package_ndc |
| spl id | 2903c621-c6e2-9048-e063-6394a90a7fa6 | id | |
| spl set id | d0880c30-54f5-4af4-ad5d-85ecae3bb9e5 | set_id | |
| unii | A4KL1HMZ7T | openfda.unii | |
| unii | 0B4FDL9I6P | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | S7YTV04R8O | openfda.unii | |
| unii | 61ZBX54883 | openfda.unii | |
| unii | 433OSF3U8A | openfda.unii | |
| unii | 535G2ABX9M | openfda.unii | |
| unii | S6G2NLH4Y7 | openfda.unii | |
| unii | B66F4574UG | openfda.unii | |
| unii | 398IYQ16YV | openfda.unii | |
| unii | E8S87O660T | openfda.unii | |
| unii | I76KB35JEV | openfda.unii | |
| unii | K73E24S6X9 | 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.