UdderBlend EFC 10

Manufacturer
BouMatic, LLC
Effective date
2013-12-01
Label type
OTC ANIMAL DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:39:44

Label at a glance#

ProductUdderBlend EFC 10
Active ingredientIODINE
Label structure3 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Concentrate for 1.0% Iodine Teat Dip

Helps reduce the spread of organisms which may cause Mastitis

NOT FOR HUMAN USE

FOR EXTERNAL USE ONLY

USE DIRECTIONS:
Do not use in concentrated form. Must dilute prior to use.

Consult your BouMatic representative for specific use
instructions and recommended dispensing equipment.


Active Ingredient (Iodine 5.0%.)

CAUTION

PRECAUTIONS SECTION

KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE

FIRST AID:
If in eyes: Hold eye open and rinse slowly and gently with water for 15-
20 minutes. Remove contact lenses, if present after the first 5 minutes,
then continue rinsing. Contact a physician immediately.

If swallowed: Have person sip a glass of water if able to swallow. Do not give anything
to an unconscious person. Do not induce vomiting. Contact a physician
immediately.

If breathing difficulty occurs: Move person to fresh
air. Contact a physician immediately.

If on skin: Take off contaminated clothing. Rinse skin with soap and water. If irritation develops and persists,
contact a physician.

Have the product container or label with you when going for treatment,
calling a physician, the emergency number listed on this label or MSDS, or
a poison control center.

PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals except as directed.

STORAGE: Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix well before use.

SEE MATERIAL SAFETY DATA SHEET

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blank LabelBlank Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
902306iodine 1 % Topical SolutionPSN3
1248600iodine 10 MG/ML Topical Solution [UdderBlend]SBD3
902306iodine 10 MG/ML Topical SolutionSCD3
902306iodine 1 % Topical SolutionSY3
1248600UdderBlend 1 % Topical SolutionSY3
1248600UdderBlend 10 MG/ML Topical SolutionSY3

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
48106-1310-3UdderBlend EFC 1056.8 L in 1 DRUMLIQUID56.83
48106-1310-5UdderBlend EFC 10208 L in 1 DRUMLIQUID2083
48106-1310-6UdderBlend EFC 101040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID10403

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48106-1310UDDERBLEND EFC 10 (IODINE) LIQUID [BOUMATIC, LLC]33 package rows20140107_444f49bd-dff0-4359-aa19-a9e7a0b56102.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
IODINEACTIVE INGREDIENT9679TC07X43
IODINEACTIVE MOIETY9679TC07X43

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
48106-131048106-1310-5, 48106-1310-3, 48106-1310-6

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.