IODINE 260 PREMIX- titratable iodine solution

Iodine 260 Premix by

Drug Labeling and Warnings

Iodine 260 Premix by is a Other medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SAFE HANDLING WARNING

Avoid breathing dust/ fume/ gas/ mist/ vapours/ spray. Wash skin thoroughly after handling. Use only outdoors or in a well-ventilated area. Wear protective gloves/ protective clothing/ eye protection/ face protection.

IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/doctor.  IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER or doctor/ physician. Wash contaminated clothing before reuse.

VETERINARY INDICATIONS

Active Pharmaceutical Ingredient

FOR INDUSTRIAL USE ONLY

OTHER SAFETY INFORMATION

Danger

Causes severe skin burns and eye damage. May cause respiratory irritation.

EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).

Principal display panel and representative container

Iodine 260 Premix

Active Pharmaceutical Ingredient

FOR INDUSTRIAL USE ONLY

DIRECTIONS:

CAUTION: For manufacturing, processing, or repackaging

ACTIVE INGREDIENT:

Titratable Iodine.............57.8%

INERT INGREDIENTS........42.2%

TOTAL...............................100.0%

NOT FOR COMMERCIAL DISTRIBUTION

7.8 US GAL (30 L)

3601370

This product may be patented: www.ecolab.com/patents

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA· tel: 1 800 392 3392

© 2021 Ecolab USA Inc · All rights reserved

Made in United States

www.ecolab.com · 778206/5300/0321

INGREDIENTS AND APPEARANCE

IODINE 260 PREMIX 
titratable iodine solution

Product Information
Product Type		Item Code (Source)	NDC: 47593-642
Route of Administration	NOT APPLICABLE

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	578 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
FORMIC ACID (UNII: 0YIW783RG1)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-642-18	30000 mL in 1 DRUM
2	NDC: 47593-642-92	113600 mL in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
drug for further processing		02/09/2022

Labeler - Ecolab Inc. (006154611)

Establishment
Name	Address	ID/FEI	Business Operations
Ecolab Inc.		064385701	analysis, api manufacture, pack, label