AlphaPro

Manufacturer
AgroChem USA, LLC
Effective date
2024-11-11
Label type
OTC ANIMAL DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:43:50

Label at a glance#

ProductAlphaPro
Active ingredientIODINE
Label structure15 sections

Storage and handling

STORAGE:  Store locked up.                        DISPOSAL: Dispose of contents/ container to an approved waste disposal plant.

Label contents#

Full prescribing information#

DESCRIPTION SECTION

ALPHAPRO

SPL UNCLASSIFIED SECTION

dip cup

spray 

foam

WARNINGS SECTION

WARNING

SPL UNCLASSIFIED SECTION

AVOID FREEZING.

KEEP OUT OF DIRECT SUNLIGHT.

CAUSES SERIOUS EYE IRRITATION.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

SPL UNCLASSIFIED SECTION

FOR FARM AND INDUSTRIAL USE ONLY.

WARNINGS AND PRECAUTIONS SECTION

PREVENTION:  Wash skin thoroughly after handling. Wear eye protection/ face protection.

FIRST AID / RESPONSE: 

IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists:  Get medical advice/ attention.          

STORAGE AND HANDLING SECTION

STORAGE:  Store locked up.                       

DISPOSAL: Dispose of contents/ container to an approved waste disposal plant.

SPL UNCLASSIFIED SECTION

EMERGENCY TELEPHONE NUMBER (Chemtrec) 800-424-9300 CCN205494

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: Iodine 0.25% (2.5 % Polyethoxy Polypropoxy Polyethoxy Ethanol - Iodine Complex) Titration via USP33 Reissue, Topical Solution

SPL UNCLASSIFIED SECTION

EMOLLIENT:  2.0%     

SPL UNCLASSIFIED SECTION

AlphaPro is made with IoPlex technology and is NPE free. 

AlphaPro is also available in a concentrated formula.

NET CONTENTS: 

LOT:

INDICATIONS & USAGE SECTION

Use AlphaPro effectively to reduce the spread of mastitis causing organisms. 

Recommended for pre milking applications.

Directions:

General Use

Ready to use.  Do not dilute.  Do not mix product with water, any other teat dips, or other product.

Use a teat dip cup to apply.  Clean dip cup just prior to use.

If cow’s teats are sore or chapped, consult a veterinarian before starting or continuing to use teat dip.

If transferred from this container to any other, make sure that the other container is thoroughly pre-cleaned and bears the proper container labeling for this product. 

If product in dip cup becomes visibly dirty, discard contents and replenish with undiluted product. Do not reuse or return any unused product to the original container.

Teat Sprays can also be foamed or sprayed using recommended equipment.

Pre Dipping Use

Perform forestripping and inspect teats for clinical mastitis.

Pre-wash teats thoroughly just prior milking with appropriate udder wash solution or pre-milking teat dip. Teats should then be dried with single-service towels

Just before each cow is milked, dip, foam, or spray, each teat full-length into the teat dip or foam cup containing product.

Allow product to stand for 30 seconds.

Wipe teats dry after dipping, using single-service towels to avoid contamination of milk.

Post Dipping Use

Immediately after each milking, use product.

Dip each teat full-length into the teat dip cup containing product.  Allow to air dry.  Do not wipe.

If outside temperature is below freezing, allow to air dry on the teat before cow leaves the parlor.

Extended Use

When a cow is being dried off, the teats should be dipped in product, once a day for 3-4 days after the last milking.

Dipping should be resumed at least twice daily one week before calving.

SPL UNCLASSIFIED SECTION

AgroChem

26 Freedom Way  Saratoga Springs, NY 12866 (518)226-4850

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
17307-3190-1AlphaPro19 kg in 1 CONTAINERSOLUTION192
17307-3190-2AlphaPro57 kg in 1 DRUMSOLUTION572
17307-3190-3AlphaPro208 kg in 1 DRUMSOLUTION2082
17307-3190-4AlphaPro1040 kg in 1 CONTAINERSOLUTION10402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17307-3190ALPHAPRO (IODINE SOLUTION) SOLUTION [AGROCHEM USA, LLC]24 package rows20241113_a903a919-d749-42e8-b48b-acdd2e1eadeb.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17307-319017307-3190-1, 17307-3190-2, 17307-3190-3, 17307-3190-4

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.