UDDERBLEND NPE FREE- iodine teat dip concentrate liquid

Udderblend NPE Free by

Drug Labeling and Warnings

Udderblend NPE Free by is a Animal medication manufactured, distributed, or labeled by BouMatic, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS AND PRECAUTIONS

CAUTION

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

INDICATIONS & USAGE

Iodine Teat Dip Concentrate

 Helps reduce the spread of organisms which may cause Mastitis

RESTRICTED DRUG (CA) - USE ONLY AS DIRECTED

USE DIRECTIONS

NOT FOR HUMAN USE

FOR EXTERNAL USE ONLY

Do not use in concentrated form. Must dilute prior to use.

To obtain a 1% iodine solution and 2% emollients, add 1 part UdderBlend to 4 parts water and mix thoroughly.

To obtain a 0.5% iodine solution and 1% emollients, add 1 part UdderBlend to 9 parts water and mix thoroughly.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UDDERBLEND NPE FREE 
iodine teat dip concentrate liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2026
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	55 g  in 1 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2026-1	18.9 L in 1 DRUM
2	NDC: 48106-2026-2	56.8 L in 1 DRUM
3	NDC: 48106-2026-3	208 L in 1 DRUM
4	NDC: 48106-2026-4	1041 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		09/01/2016

Labeler - BouMatic, LLC (124727400)

Registrant - BouMatic, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
boumatic		080073197	manufacture, api manufacture