FDA.reportPublic FDA data

Hoofshield

Manufacturer
Quat-Chem Ltd.
Effective date
2016-07-18
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:39:58

Label at a glance#

ProductHoofshield
Active ingredientCUPRIC SULFATE, ZINC SULFATE, BENZALKONIUM CHLORIDE, GLUTARAL
Label structure2 sections

Label contents#

Full prescribing information#

CORROSIVE LIQUID, ACIDIC, ORGANIC, N.O.S.UN 3265(CONTAINS GLUTARALDEHYDE) DANGERHarmful if swallowed. Causes severe skin burns and eye damage.May cause an allergic skin reaction. May cause allergy or asthma symptoms or breathing difficulties if inhaled. Ver...

WARNINGS AND PRECAUTIONS SECTION

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Representative label Hoofshield(B)25L USA-1.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69260-01269260-012-05, 69260-012-25, 69260-012-20, 69260-012-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CUPRIC SULFATELRX7AJ16DTACTIM
ZINC SULFATE89DS0H96TBACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLUTARALT3C89M417NACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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