Ovapar

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 (canonical bytes are SHA-256 checked before publication)

Brand name
Ovapar
Generic name
ANGELICA ARCHANGELICA, CAULOPHYLLUM THALICTROIDES, XANTHOXYLUM FRAXINEUM, OOPHORINUM (SUIS), APIS MELLIFICA, BELLADONNA, LACHESIS MUTUS, MAGNESIA PHOSPHORICA, SEPIA, MUREX PURPUREA
Manufacturer
Energique, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
13ecc450-0ae3-46d3-8cc7-915c74c3361a
SPL ID
0bde06ea-79eb-4660-b2f2-7e7f12347b25
Version
3
Effective date
2024-10-29
Source export date
2026-09-28
Source partition
14
Source file
https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:40:40
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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