OFB Iodine Concentrate IC

Manufacturer
DeLaval | WestAgro, Inc. | K Klean dba WestAgro, Inc.
Effective date
2018-06-28
Label type
OTC ANIMAL DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-02 00:53:57

Label at a glance#

ProductOFB Iodine Concentrate IC
Active ingredientIodine, Glycerin
Label structure18 sections

Storage and handling

STORAGE AND DISPOSAL THOROUGHLY RINSE ALL MEASURING DEVICES AND STORE OUT OF REACH OF CHILDREN. Avoid contact with food or feed.  Avoid storing near heat or open flame. Keep from freezing. If product is frozen, thaw in warm room and mix well before using. Keep container tightly closed when not in use. Do not reuse empty container. Rinse empty container before disposing in a safe manner.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

An iodine concentrate designed for use with OFB Emollient Concentrate EC for on-farm blending

Un concentrado de yodo disenado para su uso con Emollient Concentrate EC para mezclar en la finca

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:
Iodine ............................... 5.2%
Emollient* ......................... 8.5%
*from Glycerin

SPL UNCLASSIFIED SECTION

1322-E0116

I2

PART A

NPE FREE Formula

SPL UNCLASSIFIED SECTION

1322-B0413

I2

PART A

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN
!CAUTION

MANTENER FUERA DEL ALCANCE DE LOS NINOS
!CUIDADO

SPL UNCLASSIFIED SECTION

SI USTED NO PUEDE LEER ESTA ETIQUETA, POR FAVOR PIDA A ALGUIEN MAS QUE SE LA LEA ANTES DE USAR ESTE PRODUCTO

READ AND UNDERSTAND ALL INSTRUCTIONS BEFORE USING THIS PRODUCT

SPL UNCLASSIFIED SECTION

1322

SPL UNCLASSIFIED SECTION

Not for Human Use

Additional Information on Material Safety Data Sheet

SPL UNCLASSIFIED SECTION

CHEMTREC EMERGENCY NUMBER 1-800-424-9300

SPL UNCLASSIFIED SECTION

OFB Emollient Concentrate IC (Part A) is an Iodine concentrate exclusively designed for use in combination with OFB Iodine Concentrate EC (Part B) for on-farm blending / production of teat dips.  To be blended using on-farm blending equipment.

STORAGE AND HANDLING SECTION

STORAGE AND DISPOSAL

  • THOROUGHLY RINSE ALL MEASURING DEVICES AND STORE OUT OF REACH OF CHILDREN.
  • Avoid contact with food or feed.  Avoid storing near heat or open flame.
  • Keep from freezing.
  • If product is frozen, thaw in warm room and mix well before using.
  • Keep container tightly closed when not in use.
  • Do not reuse empty container.
  • Rinse empty container before disposing in a safe manner.

SPL UNCLASSIFIED SECTION

GENERAL INSTRUCTIONS

  • Do not use full-strength.
  • Consult veterinarian before starting or continuing to use teat dip if cow's teats are sore or chapped.
  • Do not use teat dip for cleaning and/or sanitizing of dairy equipment.
  • Discard any teat sanitizing solution that becomes dirty or contaminated for any reason.
  • Good dairy practices suggest the thorough cleaning and sanitizing of teats before milking to avoid contamination and assist in the control of mastitis.
  • To be mixed with OFB Iodine Concentrate EC (Part B) using programmed on-farm blending equipment.  Can be diluted to create 12 formula options.

SPL UNCLASSIFIED SECTION

FIRST AID

  • Contact with product can cause irritation to eyes.  Avoid contact with eyes.
  • Eye contact:  Flush with water.
  • If swallowed:  Do not induce vomiting.  Call a physician or poison control center immediately.

INDICATIONS & USAGE SECTION

USE DIRECTIONS

Pre-Dipping

  • Remove excess organic debris and forestrip.
  • Dip or spray cow's teats with properly diluted On-Farm Blending Concentrate.
  • Allow a 30 second contact time.
  • Dry teats thoroughly with a clean, single-service paper towel.
  • Attach milker unit.

Post-Dipping

  • Immediately after removing milker unit, dip or spray each teat with properly diluted On-Farm Blending Concentrate.
  • Before exposing cow's teats to below freezing temperatures, the teats should be thoroughly dry to reduce the potential of frostbite.  Failure to follow these instructions may result in frozen teats and injured animals.

SPL UNCLASSIFIED SECTION

DILUTION CHART
%
Emollient
0.25% Iodine0.5% Iodine0.75% Iodine1.0% Iodine
OFB
(PART A)
Iodine
Conc./
Gal.
OFB
(PART B)
Emollient
Conc./
Gal.
Water /
Gal.
OFB
(PART A)
Iodine
Conc./
Gal.
OFB
(PART B)
Emollient
Conc./
Gal.
Water /
Gal.
OFB
(PART A)
Iodine
Conc./
Gal
.
OFB
(PART B)
Emollient
Conc./
Gal.
Water /
Gal.
OFB
(PART A)
Iodine
Conc./
Gal.
OFB
(PART B)
Emollient
Conc./
Gal.
Water /
Gal.
24.582.7892.659.162.0188.8313.741.2585.0218.320.4881.20
3.513.743.9082.36
54.588.0887.349.167.3283.5213.746.5679.7118.325.7975.89
104.5816.9378.499.1616.1774.6713.7415.4170.8618.3214.6467.04
1213.7418.9567.3218.3218.1863.50
1418.3221.7259.96

SPL UNCLASSIFIED SECTION

IMPORTANT!

  • 0.25% teat dip must be mixed on demand.
  • 0.5% - 1.0% teat dip must be used within two weeks after mixing.
  • Discard unused mixtures after above noted times.

SPL UNCLASSIFIED SECTION

Manufactured for: DeLaval, Inc.
11100 N. Congress Avenue
Kansas City, MO 64153
Phone: 816-891-7700
Manufactured by: WestAgro, Inc.
©2018, Made in USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-137320461167184GTIN-13: 7320461167184
EAN-13: 7320461167184
GTIN storage (14 digits): 07320461167184
OFB Iodine Conc IC Label.jpg

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GlycerinACTIVE INGREDIENTPDC6A3C0OX4
IodineACTIVE INGREDIENT9679TC07X44
GlycerinACTIVE MOIETYPDC6A3C0OX4
IodineACTIVE MOIETY9679TC07X44
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSL4
DOCUSATE SODIUMINACTIVE INGREDIENTF05Q2T2JA04
POLOXAMER 335INACTIVE INGREDIENTG6DQL26D504
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32I4
SODIUM IODIDEINACTIVE INGREDIENTF5WR8N145C4
WaterINACTIVE INGREDIENT059QF0KO0R4

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55756-32255756-322-01, 55756-322-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 5 · 249 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRASPINALADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ICAPSULE, LIQUID FILLED / ORAL1.5 mgExact identifier — unii candidate
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ANHYDROUS CITRIC ACIDANHYDROUS CITRIC ACIDXF417D3PSLGEL / TOPICAL3 mgExact identifier — unii candidate
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ANHYDROUS CITRIC ACIDANHYDROUS CITRIC ACIDXF417D3PSLPASTE / ORAL26 mgExact identifier — unii candidate
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ANHYDROUS CITRIC ACIDANHYDROUS CITRIC ACIDXF417D3PSLINJECTION, SOLUTION / INTRAMUSCULAR25 mgExact identifier — unii candidate
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ANHYDROUS CITRIC ACIDANHYDROUS CITRIC ACIDXF417D3PSLAEROSOL, FOAM / TOPICAL6 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION, SOLUTION / INTRAVENOUS78 mgExact identifier — unii candidate
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DOCUSATE SODIUMDOCUSATE SODIUMF05Q2T2JA0INJECTION / INTRAMUSCULAR0.02 %w/vExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ICAPSULE, DELAYED RELEASE / ORAL0.25 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IOINTMENT, AUGMENTED / TOPICAL0.11 %w/wExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IGEL, METERED / TRANSDERMAL350 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / NASAL20 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISUSPENSION, EXTENDED RELEASE / INTRALESIONALADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRACAVITARYADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IAEROSOL, METERED / RESPIRATORY (INHALATION)ADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / EPIDURALADJ PHExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ICONCENTRATE / ORAL10 mg/5mlExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IGEL / TOPICAL70 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32IINJECTION / INTRAMUSCULAR176 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ISOLUTION / RESPIRATORY (INHALATION)8 %w/vExact identifier — unii candidate
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ANHYDROUS CITRIC ACIDANHYDROUS CITRIC ACIDXF417D3PSLFILM, SOLUBLE / ORAL7 mgExact identifier — unii candidate
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SODIUM HYDROXIDESODIUM HYDROXIDE55X04QC32ICREAM / VAGINAL0.19 %w/wExact identifier — unii candidate
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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.