Della Soft

Manufacturer
DeLaval Inc. | West Agro, Inc.
Effective date
2026-03-09
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:46:35

Label at a glance#

ProductDella Soft
Active ingredientIODINE
Label structure4 sections

Label contents#

Full prescribing information#

Della Soft

STATEMENT OF IDENTITY SECTION

Storage: Store at room tepmerature

Approval No.: 12 Chiku A No. 833

Veterinary Pharmaceutical Product - Teat Disinfectant for Cattle

Disinfection and sanitization of bovine teats.

Use the solution undiluted.

Pour into a cup or similar container and briefly immerse the teats after each milking.

Ingredients and Quantities (per 100g)

Iodine-glycerin complex solution.....1.82 g (Available iodine: 0.5g)

Sodium iodide.... 0.10 g

Glycerin..... 1.07 g

Add image transcription here...

Precautions to Be Observed

WARNINGS AND PRECAUTIONS SECTION

This product must be used only for the purposes specified in its indications and effects.

Follow the specified dosage and administration strictly.

Precautions for Handling and Disposal:

Use this product undiluted, and shake gently before use to ensure thorough mixing. Do not use metal containers, as this product is corrosive.

Do not mix this product with other disinfectants.

Organic matter consumes available iodine; therefore avoid contamination.

If a large amount of milk or other organic matter is mixed in, discard the solution and refill the container with fresh product.

Do not reuse the product if it has been left standing for a long period after use.

Keep Out of Reach of Children. Store at room temperature, avoiding direct sunlight.

If the product freezes in cold environments, warm it to room temperature and liquefy it before use.

To avoid misuse and maintain product quality, do not transfer the product to another container.

In case of leakage, rinse with plenty of water. When disposing of unused product, avoid contaminating the environment or water systems, and follow local regulations.

Dispose of used containers in accordance with local ordinances.

Precautions During Use

USER SAFETY WARNINGS SECTION

Wear protective goggles when using this product.

If the product gets into your eyes, rinse immediately with plenty of water, including the inner eyelids, for at least 15 minutes. If eye irritation persists, seek medical attention.

Wear long-sleeved clothing and protective gloves when handling the product. If the product comes into contact with skin, wash thoroughly with soap and plenty of water, and remove contaminated clothing and shoes. Do not ingest this product.

If accidentally swallowed, give plenty of water, induce vomiting if appropriate, and seek medical attention immediately.

Ensure adequate ventilation during use. If vapors are inhaled, move to an area with fresh air.

Precautions for Cattle:

Adverse reactions: In rare cases, hypersensitivity such as rash may occur. If such symptoms appear, discontinue use and consult a veterinarian.

For external use only. Do not use this product for pre-milking disinfection.

Net volume:

Lot No.:

Expiration date:

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
55756-784-01Della Soft208 L in 1 DRUMSOLUTION2081
55756-784-02Della Soft56.8 L in 1 PAILSOLUTION56.81
55756-784-08Della Soft19 L in 1 PAILSOLUTION191

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
55756-78455756-784-01, 55756-784-02, 55756-784-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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.