FS EDX-502

Manufacturer
Genex Cooperative, Inc. | ProActive Solutions USA, LLC
Effective date
2024-01-12
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:42:46

Label at a glance#

ProductFS EDX-502
Active ingredientIODINE
Label structure2 sections

Label contents#

Full prescribing information#

FS EDX-502

DESCRIPTION SECTION

EDX-502™ is an iodine teat dip to aid in the prevention of the spread of
mastitis causing organisms.
Directions:
Use full strength.
Pre-Dipping: Just before milking, make sure the teats are clean and dry. Dip each
teat in undiluted EDX-502™. Allow to soak for 15-30 seconds. Dry with a single
service towel and attach milker units.
Post-Dipping: : Immediately after removing inflations, dip each teat in undiluted
EDX-502™. Allow teat to air dry. Do not wipe. Replace the solution if it becomes
visibly dirty.

CAUTION
Hazard statement(s):
May be harmful if swallowed. May cause eye irritation.
Precautionary statement(s):
Do not eat, drink or smoke while using this product. Wear protective clothing, and eye
and face protection.
Hazards not otherwise classified: None Known
First Aid:
General Advice: May cause eye irritation with corneal injury and result in impairment
of vision. External: If irritation occurs, flush with plenty of cool, running water for at
least 15 minutes while removing contaminated clothing and shoes. Wash clothing
before reuse.
Eyes: Immediately flush with plenty of cool, running water. Remove contact lenses;
then continue flushing for at least 15 minutes, holding eyelids apart.
Internal: Call a physician immediately. If swallowed, do not induce vomiting. Rinse
mouth, then immediately drink one or two large glasses of water or milk. Never give
anything by mouth to an unconscious person.
Inhalation of vapors: Should not occur with proper use of this product.
Most important symptoms/effects, acute and delayed: None known
Immediate medical attention and special treatment needed, if any: None known
FOR CHEMICAL EMERGENCIES: CALL CHEMTREC 1-800-424-9300

FS EDX 502

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FS EDX-502FS EDX-502

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86193-4163-1FS EDX-5021046.56 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID1046.561

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86193-4163FS EDX-502 (IODINE) LIQUID [GENEX COOPERATIVE, INC.]11 package rows20240113_ecb48aab-a14d-4bcc-b7cb-2f6ea816615a.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86193-416386193-4163-1

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
IODINE9679TC07X4ACTIB

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 · 11 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IodineIODINENice-Pak Products, LLC857f13fe-51c9-4e5b-b5e2-a981dedabf712026-03-12Warnings, Adverse reactionsName fallback
generic name: IODINE
IodineIODINEUnited Natural Foods, Inc. dba UNFI8e840855-d210-4a99-b73f-6c69dcf2b6fb2026-02-16WarningsName fallback
generic name: IODINE
IODDO IODINEIODINEEVI LABS4af8552c-1f2b-84ad-e063-6394a90abb622026-02-16WarningsName fallback
generic name: IODINE
IodineIODINEWalgreen Co.d3d44c9f-4eb6-4e5b-9943-c0f80f06952d2026-02-12Warnings, Adverse reactionsName fallback
generic name: IODINE
IodiumIODINEBoiron85cd5e7a-52b6-0bb7-e053-2a91aa0aaa142023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd0c27-7859-5fd8-e053-2a91aa0a7c692023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd0c27-782d-5fd8-e053-2a91aa0a7c692023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron724cb010-7c5d-11e6-8589-424c583030312023-11-13Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd3f96-b800-f192-e053-2991aa0aee982023-02-20Name fallback
generic name: IODINE
IodiumIODINEBoiron85cd5e7a-52a7-0bb7-e053-2a91aa0aaa142023-01-23Name fallback
generic name: IODINE
IodiumIODINEBoiron85ccdc3f-5dd9-a5b1-e053-2a91aa0a8a0c2023-01-05Name fallback
generic name: IODINE

Reported adverse events (FAERS/openFDA)#

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