FDA.reportPublic FDA data

Zeranol

Manufacturer
BioVectra Inc.
Effective date
2022-10-28
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:50:22

Label at a glance#

ProductZeranol
Active ingredientZeranol
Label structure1 sections

Label contents#

Full prescribing information#

PRINCIPAL DISPLAY PANEL - Shipping Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BioVectra
Zeranol

!

No GHS
Pictogram

WARNING
See Safety Data Sheet

Hazards: Causes skin and eye irritation. Suspected of
damaging fertility or the unborn child. May cause damage to
liver, endocrine, nervous, or reproductive systems through
prolonged or repeated exposure.

Precaution: Do not breath dust. Use personal protective
equipment as required and wash thoroughly after handling. Do
not eat, drink, or smoke when using this product. If on skin,
wash thoroughly with soap and water. If in eyes, rinse for at
least 15 minutes with water. Get medical attention if feeling
unwell.

Cat. No. 7037
Gross Weight:
Tare Weight:
Net Weight:
Lot:
Store @ 15-30°C
M.W. 322.40
Retest/Expiry Date

Date of Manufacture

CAS 26538-44-3

Made in

BioVectra Inc. 11 Aviation Ave., Charlottetown, PE C1E 0A1 (866) 883-2872
www.biovectra.com

Shipping Label
Shipping Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63474-600-302020-02-06C16284748780-19d75b9d0-f2e0-f424-e053-dadaa90a57ceZeranol
63474-600-302020-01-31C16284748780-19d75b9d0-f2e0-f424-e053-dadaa90a57ceZeranol

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63474-60063474-600-30

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Zeranol76LO2L2V39ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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