FDA.reportPublic FDA data

NU-KOTE

Manufacturer
Tetradyne LLC
Effective date
2015-11-09
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:29:59

Label at a glance#

ProductNU-KOTE
Active ingredientIODINE, GLYCERIN
Label structure3 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION


USE DIRECTIONS:
Use at full strength, do not dilute.

For post-dipping: Dip Entire teat in NU-KOTE.  Allow to air dry.  If solution in cup becomes visibly dirty or cloudy, then replenish with NU-KOTE at full strength.  Do not return unused product to original container.

NOTE: This product does not contain NPE (Nonylphenol Ethoxylate) Surfactant.

PROTECT FROM FREEZING
IF FROZEN:  SHAKE VIGOROUSLY
AFTER THAWING

WARNINGS AND PRECAUTIONS SECTION

WARNING:  CONTAINS IODINE.

Avoid contamination of food.  Avoid contact with eyes.  Not for internal use. Not for human use.

KEEP OUT OF REACH OF CHILDREN!

OBSERVE LABEL DIRECTIONS

FIRST AID:

INTERNAL: If swallowed, do not induce vomiting.

Drink large quantities of water.  See physician immediately.


EYES: Flush eyes with clear water for 15 minutes.
If irritated, obtain medical guidance.

GET MEDICAL ATTENTION IMMEDIATELY.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NU-KOTE

BARRIER TEAT DIP

This product, when properly used, is effective as an aid
in reducing the spread of organisms which may cause
mastitis.

Active Ingredient..........1.00% Available Iodine (provides 10,000 ppm titratable iodine)
pH.....................................Minimum 4.0
Emollients........................15% Glycerin

Lot#:
Exp. Date:
Net contents:

Manufactured For:

Tetradyne LLC
PO Box 17003
Reno, NV  86511

Package LabelPackage Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
GLYCERINACTIVE INGREDIENTPDC6A3C0OX1
IODINEACTIVE INGREDIENT9679TC07X41
GLYCERINACTIVE MOIETYPDC6A3C0OX1
IODINEACTIVE MOIETY9679TC07X41

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66399-90766399-907-01, 66399-907-02, 66399-907-03, 66399-907-04, 66399-907-05, 66399-907-06, 66399-907-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
IODINE9679TC07X4ACTIB
GLYCERINPDC6A3C0OXACTIB

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.