FDA.reportPublic FDA data

Udderstar Barrier Activator

Manufacturer
Knapp Manufacturing, Inc. | BouMatic, LLC
Effective date
2023-02-20
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:41:53

Label at a glance#

ProductUdderstar Barrier Activator
Active ingredientLACTIC ACID
Label structure6 sections

Storage and handling

Store closed container in a cool, dry location away from sources of heat. If product becomes frozen, thaw and mix well before use.

Label contents#

Full prescribing information#

Summary of effectiveness

SUMMARY OF SAFETY AND EFFECTIVENESS

Helps reduce the spread of organisms which may
cause Mastitis

Instructions for use

INSTRUCTIONS FOR USE SECTION

POST-DIPPING: After milking, spray or dip entire teat with this product. Allow to air dry.
Note: If solution in cup becomes visibly dirty, replenish with a fresh mixture of this product. Do
not return unused product to original container.

Safe Handling

SAFE HANDLING WARNING SECTION

NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
Do not mix with any chemicals other than UdderStar Barrier Base.
In a well-ventilated area, mix equal parts UdderStar Barrier Activator and UdderStar Barrier

General Precautions

GENERAL PRECAUTIONS SECTION

CAUTION
KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE

Avoid eye contact. Do not ingest. Do not mix with any chemicals except as directed.

Storage and Handling

STORAGE AND HANDLING SECTION

Store closed container in a cool, dry location away from sources of heat. If product
becomes frozen, thaw and mix well before use.

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43104-2017-1Udderstar Barrier Activator3914 g in 1 PACKAGELIQUID39141
43104-2017-2Udderstar Barrier Activator19570 g in 1 PACKAGELIQUID195701
43104-2017-3Udderstar Barrier Activator58710 g in 1 PACKAGELIQUID587101
43104-2017-4Udderstar Barrier Activator117421 g in 1 PACKAGELIQUID1174211
43104-2017-5Udderstar Barrier Activator215271 g in 1 PACKAGELIQUID2152711
43104-2017-6Udderstar Barrier Activator1076359 g in 1 PACKAGELIQUID10763591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43104-2017UDDERSTAR BARRIER ACTIVATOR (SODIUM CHLORITE TEAT DIP) LIQUID [KNAPP MANUFACTURING, INC.]16 package rows20230222_015c8b9d-bb5f-47d2-afbd-b57e655d8388.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43104-201743104-2017-1, 43104-2017-2, 43104-2017-3, 43104-2017-4, 43104-2017-5, 43104-2017-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
LACTIC ACID33X04XA5ATACTIB
SORBITOL506T60A25RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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