ZURALAC SD- teat dip liquid 
Zurex PharmAgra, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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DIRECTIONS FOR USE:

IMPORTANT: Always use ZuraLac SD as directed ZuraLac SD is a ready-to-use (RTU) product that should not be diluted or mixed with water If used with a dip cup, pour ZuraLac SD into a clean dip cup and apply to cow teats after milking If product in dip cup becomes visibly dirty, discard remaining product, thoroughly clean dip cup, and replenish with ZuraLac SD

Post-Milking Treatment:

Immediately after milking, dip each teat with full strength ZuraLac SD

Allow to air dry

PRECAUTION: AS With any teat treatment, if teats become chapped or irritated, discontinue use of the product and have the condition examined and, if necessary, treated by a veterinarian.

ACTIVE INGREDIENT(S):

Tnsodium citrate ......10.0%

* Contains 5% emollients

Causes serious eye irritation.

PRECAUTIONARY STATEMENTS:

Keep out of reach of children. Read label before use. Do not breathe dusts or mists. Get medical advice and attention if you feel unwell.

Collect spillage. Store in a dry place.

Store in a closed container.

FIRST AID

IF IN EYES: Rinse cautiously with water for several minutes. Remove Contact lenses, if present and easy to do. Continue Rinsing. IF ON SKIN: Wash with plenty of water.

IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing

IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

Manufactured for ZUREX PharmAgra(wnww.zurexpharmagra com) by DeVere(1923 Beloit Avenue, Janesville WI 53546).

See safety data sheet for more information.

EMERGENCY PHONE: 1-800-535-5053

U.S. Patent No. 9,040,023

Label

ZURALAC SD 
teat dip liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:50005-3022
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CITRATE (UNII: 1Q73Q2JULR) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) SODIUM CITRATE10 g  in 1 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50005-3022-13.8 L in 1 JUG
2NDC:50005-3022-256.8 L in 1 DRUM
3NDC:50005-3022-3208 L in 1 DRUM
4NDC:50005-3022-41040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/01/201509/16/2019
Labeler - Zurex PharmAgra, LLC (078463043)
Registrant - Zurex PharmAgra, LLC (078463043)
Establishment
NameAddressID/FEIBusiness Operations
Zurex PharmAgra, LLC078463043api manufacture

Revised: 9/2019
 
Zurex PharmAgra, LLC