BULK IODINE CONCENTRATE- iodine teat dip liquid

Bulk Iodine Concentrate by

Drug Labeling and Warnings

Bulk Iodine Concentrate by is a Animal medication manufactured, distributed, or labeled by BOUMATIC, LLC, Knapp Manufacturing, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Claim of effectiveness.

Helps reduce the spread of organisms
which may cause Mastitis

Use Directions

NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
Do not use in concentrated form.
Use only as directed.
For use only with BouMatic mixing
systems.
Reference procedure manual for
specific mixing instructions.

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 SDS, or a poison control
center.

Precautions & Hazards

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.

label

INGREDIENTS AND APPEARANCE

BULK IODINE CONCENTRATE 
iodine teat dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2051
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	7.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2051-1	1076359 g in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/02/2023

Labeler - BOUMATIC, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
BOUMATIC, LLC		124727400	api manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Knapp Manufacturing, Inc.		063012827	manufacture