ULTRA-GUARD ACTIVATOR solution

ULTRA-GUARD ACTIVATOR by

Drug Labeling and Warnings

ULTRA-GUARD ACTIVATOR by is a Animal medication manufactured, distributed, or labeled by IBA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Organic Acids...........2.85%

INERT INGREDIENTS

Contains A Special Emollient System

INDICATIONS AND USAGE

GENERAL RECOMMENDATIONS

To make a ready-to-use solution of Ultra-Guard Sanitizing Barrier Teat dip, add equal volumes of Ultra-Guard Activator and Ultra-Guard Base into a clean dip cup/container and mix until the color is uniform throughout. Do not dilute. Mix only the amount needed for one milking of the herd. Discard any unused teat dip. Do not mix with any other products.

RECOMMENDED PROCEDURES FOR TEAT SANITATION
POST-MILKING (POST-DIPPING)
Immediately after milking, dip all teats full length with READY-TO-USE ULTRA-GUARD SANITIZING BARRIER TEAT DIP. Ensure good coverage of all sides of the teats and teat orifices. Allow to dry. Do not wipe. Do not turn cows out in freezing weather until teat dip is completely dry.

NOTE: Before milking, use a compatible teat dip or udder wash to thoroughly clean the teats.

WARNING

Do not dilute this product.
Do not return teat dip left in the teat dipper to storage container.
Ensure that dipped teats are dry before exposing the animals to weather conditions which may cause damage to the teats.
Store at room temperature. Always store away from direct sunlight.

Protect this product from freezing. However, freezing will not affect ULTRA-GUARD ACTIVATOR provided that the contents are thawed completely and agitated thoroughly before mixing base and activator together.

CAUTION: KEEP OUT OF REACH OF CHILDREN.
AVOID CONTACT WITH FOOD. DO NOT TAKE INTERNALLY.

FIRST AID PROCEDURES

EYE CONTACT: Rinse cautiously with fresh, tepid water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing for 15 minutes. Get immediate medical advice/attention. SKIN CONTACT: For RTU products wash any sensitive areas. INGESTION: Do not induce vomiting. Never give anything by mouth to an unconscious person. Drink large amounts of water. If vomiting occurs, keep airways open. Keep head lower than the hips to prevent aspiration into the lungs. Get immediate medical advice/attention.

ALWAYS SEEK IMMEDIATE MEDICAL ATTENTION

FOR MEDICAL EMERGENCIES CALL 1-800-424-9300

ULTRA-GUARD ACTIVATOR

INGREDIENTS AND APPEARANCE

ULTRA-GUARD ACTIVATOR 
ultra-guard activator solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 29983-0087
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	28.5 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
UREA (UNII: 8W8T17847W)

Product Characteristics
Color	orange	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29983-0087-4	18.9 L in 1 DRUM
2	NDC: 29983-0087-6	56.7 L in 1 DRUM
3	NDC: 29983-0087-8	207.9 L in 1 DRUM
4	NDC: 29983-0087-9	1039.5 L in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/15/2022

Labeler - IBA (019494160)