Quartermate A

Manufacturer
West Agro, Inc.
Effective date
2026-03-11
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:46:35

Label at a glance#

ProductQuartermate A
Active ingredientiodine
Label structure4 sections

Label contents#

Full prescribing information#

Quartermate A

OTC - ACTIVE INGREDIENT SECTION

Contains available iodine 0.1% and glycerin 2%

Volume:

This teat dip is environmentally friendly and produced using two U.S. patented technologies.

IO-MAXX technology provides rapid and strong bactericidal activity.

ACT technology keeps teats consistently soft.

Composition/Content per 100 g

Glycerin-iodine complex 0.33 g

Sodium iodate 0.20 g

Glycerin 1.84g

Precautions to Be Observed

PRECAUTIONS SECTION

General Precautions:

Use this product only for the purposes specified under indications and effects. Follow the designated dosage and administration strictly.

Handling and Disposal Precautions:

Do not use metal cups because the product is corrosive. SHake well before use. Milk and other organic matter consume avilable iodine and reduce the disinfecting effect. If a large amount of milk or organic matter enters the container, discard the solution and refille with a fresh one. Store out of reach of children. Avoid contact with food, feed, clothing, and children's toys. Store tightly sealed in a place away from direct sunlight, high temperature, and humidity, and where freezing does not occur. Do not store near fire or heat sources. If frozen, warm to room temperature and mix before use. To avoid misuse and maintain product quality, do not transfer the product to another container. Dispose of used containers according to local regulations. When discarding the product, ensure it does not contaminate the environment or water systems and dispose of it according to local regulations.

Precautions During Use

WARNINGS AND PRECAUTIONS SECTION

If hypersensitivity symptoms such as rash or itching occur, discontinue use immediately and consult a physician. Wear rubber gloves when handling the product to avoid skin contact. If the product adheres to the skin, rinse immediately with running water.

Avoid eye contact. If the product gets into the eyes, do not rub - rinse immediately with running water. After rinsing for about 5 minutes, remove contact lenses if worn and continue rinsing. Bring this product and seek prompt medical attention.

Avoid accidental ingestion. If swallowed, give plenty of water to induce vomiting when appropriate and seek immediate medical attention.

Precaustions for cattle:

Hypersensitivity reactions such as rash may occur, discontinue use if such symptoms appear. If the teat has wounds or cracks, consult a veterinarian before use. Teat immersion time should be 15-30 seconds. Before teats dry, lying down may cause manure or bedding to adhere. Keep cows standing until teats are completely dry. In cold climates, teats may be at risk of frostbite; after dipping, wait about one minute, then wipe teats with a new paper towel or dry indoors at room temperature.

Other handling precautions:

Use indulated. Use fresh solution for each milking. Clean cups or non-return dipper devices thoroughly before use.

Clean all equipment thoroughly after use.

Use within expiry date printed on the package.

Contact Nippon Zenyaku Kogyo Co., Ltd. 1-1 Hirano-ue, Sasagawa, Asaka-machi, Koriyama-shi, Fukushima 963-0196 Japan

Toll-free 0120-452-793 Hours: 9:00 - 17:00 (excluding weekends and company holidays)

Veterinarians, pharmacists, and other healthcare professionals who become aware of any disease, injury, or death suspected to be related to this product, or infections suspected to be associated with its use, should contact the above information center and also report to the National Veterinary Assay Laboratory (www.maff.go.jp/nval/yakutou/fukusayo/sousa/index.html).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label ImageProduct Label Image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
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ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
33392-703-01Quartermate A208 L in 1 DRUMSOLUTION2081
33392-703-02Quartermate A57 L in 1 PAILSOLUTION571
33392-703-08Quartermate A19 L in 1 PAILSOLUTION191

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
33392-70333392-703-01, 33392-703-02, 33392-703-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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.