Aura Concentrate

Manufacturer
AgroChem USA, LLC.
Effective date
2024-07-17
Label type
OTC ANIMAL DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:43:23

Label at a glance#

ProductAura Concentrate
Active ingredientGLYCERYL LAURATE, LACTIC ACID
Label structure13 sections

Storage and handling

STORAGE:  Store  locked  up.                                                      DISPOSAL:  Dispose  of  contents/ container  to  an  approved  waste  disposal  plan

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

AURA CONCENTRATE 

SPL UNCLASSIFIED SECTION

TEAT  DIP CONCENTRATE

WARNINGS SECTION

DANGER

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

WARNINGS AND PRECAUTIONS SECTION

NOT  FOR  HUMAN  USE.

AVOID  FREEZING.

KEEP  OUT  OF  DIRECT  SUNLIGHT.

CAUSES  SKIN  IRRITATION.

CAUSES  SERIOUS  EYE  DAMAGE.

FOR  FARM  AND  INDUSTRIAL  USE  ONLY

PREVENTION:  Wear  protective  gloves.  Wear  eye  or  face  protection.  Wash  hands  thoroughly  after  handling.

FIRST AID / RESPONSE: 

IF  ON  SKIN:  Wash  with  plenty  of  water.  If  skin  irritation  occurs:  Get  medical  advice  or  attention.  Take  off  contaminated  clothing  and  wash  it  before  reuse.

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.

STORAGE AND HANDLING SECTION

STORAGE:  Store  locked  up.                                                     

DISPOSAL:  Dispose  of  contents/ container  to  an  approved  waste  disposal  plan

SPL UNCLASSIFIED SECTION

EMERGENCY  TELEPHONE  NUMBER  (CareChem 24)  1-215-207-0061                                                                                   Toll  Free:  1-866-928-0789

OTC - ACTIVE INGREDIENT SECTION

ACTIVE  INGREDIENTS  (when  diluted  1:3):  Glycerol  Monolaurate 0.25%, Lactic  Acid 2.5% 

INACTIVE INGREDIENT SECTION

EMOLLIENTS  (when  diluted  1:3):  7.5%

SPL UNCLASSIFIED SECTION

NDC: 17307-3022-3

NET CONTENTS:  55 GALLON (208.2L)

Use  Aura  Concentrate  effectively  to  reduce  the  spread  of  mastitis  causing  organisms.   Aura  Concentrate  is  suitable  for  use  as  a  pre  or  post  dip.

INSTRUCTIONS FOR USE SECTION

DIRECTIONS:

IMPORTANT:  CONCENTRATE  MUST  BE  DILUTED  WITH  CLEAN  WATER  PRIOR  TO  USE.  RECOMMENDED  DILUTION  IS  (1:3).  MIX  (1)  PART  AURA  TO  (3)  PARTS  OF  WATER.  MIX  WELL  PRIOR  TO  USE.

General Use

Use  a  teat  dip  cup  to  apply.  Clean  dip  cup  just  prior  to  use.

If   cow’s  teats  are  sore   or   chapped,  consult  a  veterinarian  before  starting  or   continuing  to  use  teat  dip.

If   transferred  from  this   container   to   any  other,  make   sure  that  the   other   container  is  thoroughly  pre-cleaned  and  bears  the  proper  container   labeling  for   this  product. 

If   product  in  dip  cup  becomes  visibly  dirty,  discard  contents  and  replenish  with  undiluted  product.  Do  not  reuse  or  return  any  unused  product  to  the  original  container.

This  product  can  also  be  foamed  or  sprayed  using  recommended  equipment.

Pre Dipping  Use

Perform  forestripping  and  inspect  teats  for  clinical  mastitis.

Pre-wash  teats  thoroughly  just  prior  to  milking  with   appropriate   udder   wash  solution  or   pre-milking  teat  dip.  Teats  should  then  be  dried  with  single-service  towels.

Just  before  each  cow  is  milked,  dip,  foam,  or  spray,  each  teat  full-length  into  the  teat  dip  or  foam  cup  containing  product.   Allow  product  to  stand  for  30  seconds.

Wipe  teats  dry  after   dipping,  using  single-service  towels  to  avoid  contamination  of  milk.

Post Dipping  Use

Immediately  after  each  milking,  use  product.

Dip  each  teat  full-length  into  the  teat  dip  cup  containing  product.  Allow  to  air  dry.  Do  not  wipe.

If  outside  temperature  is  below  freezing,  allow  to  air   dry  on  the  teat  before  cow  leaves  the  parlor.

Extended  Use

When  a  cow  is  being  dried  off, the  teats  should  be  dipped  in  product,  once  a  day  for  3-4  days   after the  last  milking.  Dipping  should  be  resumed  at  least  twice  daily  one  week  before  calving.

SPL UNCLASSIFIED SECTION

Manufactured By:

AgroChem USA, LLC 26 Freedom Way • Saratoga Springs, NY 12866 • (518)226-4850

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LACTIC ACID, UNSPECIFIED FORM Pharmacologic Class Indexing1Indexing - Pharmacologic Class20220121

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17307-3022-1Aura Concentrate19 kg in 1 CONTAINERSOLUTION195
17307-3022-2Aura Concentrate57 kg in 1 DRUMSOLUTION575
17307-3022-3Aura Concentrate208 kg in 1 DRUMSOLUTION2085
17307-3022-4Aura Concentrate1003 kg in 1 CONTAINERSOLUTION10035

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17307-3022AURA CONCENTRATE (LACTIC ACID TEAT DIP) SOLUTION [AGROCHEM USA, LLC.]54 package rows20240718_0dd53e1e-840f-4153-9108-d3ba5c2e36aa.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17307-302217307-3022-1, 17307-3022-2, 17307-3022-3, 17307-3022-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.