FDA.reportPublic FDA data

OLLOPETS WORMS

Manufacturer
SEVENE USA
Effective date
2026-02-18
Label type
OTC ANIMAL DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:37:39

Label at a glance#

ProductOLLOPETS WORMS
Active ingredientARTEMISIA ABROTANUM FLOWERING TOP, ARTEMISIA VULGARIS ROOT, ARTEMISIA CINA PRE-FLOWERING TOP, DRYOPTERIS FILIX-MAS ROOT, INDIGOFERA TINCTORIA WHOLE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SCHOENOCAULON OFFICINALE SEED, TEUCRIUM MARUM
Label structure2 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT HPUS

OTC - ACTIVE INGREDIENT SECTION

Abrotanum.........................................30K
Artemisia vulgaris ..............................30K
Cina ...................................................30K
Filix mas ............................................30K
Indigo.................................................30K
Natrum phosphoricum ......................30K
Sabadilla............................................30K
Teucrium marum ...............................30K

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

box_30ml_ollopets_wormsbox_30ml_ollopets_wormsbox_30ml_ollopets_wormsbox_30ml_ollopets_wormslabel_30ml_ollopets_wormslabel_30ml_ollopets_worms

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-2004-1OLLOPETS WORMS30 mL in 1 BOTTLE, DROPPERSOLUTION307

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76472-200476472-2004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARTEMISIA ABROTANUM FLOWERING TOPQG07G580U0ACTIB
ARTEMISIA VULGARIS ROOT32MP823R8SACTIB
ARTEMISIA CINA PRE-FLOWERING TOP28M1820ACTACTIB
DRYOPTERIS FILIX-MAS ROOTC0ZK0RRF5XACTIB
INDIGOFERA TINCTORIA WHOLE6DPG273RYPACTIB
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE70WT22SF4BACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
TEUCRIUM MARUM10464S0TAAACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AbrotanumARTEMISIA ABROTANUM FLOWERING TOPBoiron81448355-1fc0-28a4-e053-2991aa0a23e42024-02-28Name fallback
generic name: ARTEMISIA ABROTANUM FLOWERING TOP
AbrotanumARTEMISIA ABROTANUM FLOWERING TOPBoiron124efd64-13eb-7ef1-e063-6294a90a9d5e2024-02-26Name fallback
generic name: ARTEMISIA ABROTANUM FLOWERING TOP

Reported adverse events (FAERS/openFDA)#

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