Gladiator Barrier Activator

Manufacturer
BouMatic, LLC
Effective date
2012-01-01
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:39:29

Label at a glance#

ProductGladiator Barrier Activator
Active ingredientLACTIC ACID
Label structure3 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

CHLORINE DIOXIDE TEAT DIP ACTIVATOR

Helps reduce the spread of organisms
which may cause Mastitis

USE DIRECTIONS

NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY

Do not mix with any chemicals other than
GLADIATOR™ BARRIER BASE.

In a well-ventilated area, mix equal parts
GLADIATOR™ BARRIER BASE and GLADIATOR
™ BARRIER ACTIVATOR. After mixing,
the ready-to-use product will yield a 1%
Chlorine Dioxide solution. Do not mix more
product than will be used in 24-hours.

POST-DIPPING: After milking, 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.

Active Ingredient (Lactic Acid 1%)
Emollients (Glycerin 8%, Sorbitol 8%)

CAUTION

PRECAUTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

blank labelblank label

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
48106-1155-1Gladiator Barrier Activator3.8 L in 1 DRUMLIQUID3.81
48106-1155-2Gladiator Barrier Activator18.9 L in 1 DRUMLIQUID18.91
48106-1155-3Gladiator Barrier Activator56.8 L in 1 DRUMLIQUID56.81
48106-1155-4Gladiator Barrier Activator114 L in 1 DRUMLIQUID1141
48106-1155-5Gladiator Barrier Activator208 L in 1 DRUMLIQUID2081
48106-1155-6Gladiator Barrier Activator1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID10401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48106-1155GLADIATOR BARRIER ACTIVATOR (LACTIC ACID) LIQUID [BOUMATIC, LLC]16 package rows20120529_537f8c0c-01ee-4b2f-8cee-9297deb00761.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
LACTIC ACIDACTIVE INGREDIENT33X04XA5AT1
LACTIC ACIDACTIVE MOIETY33X04XA5AT1
UREAINACTIVE INGREDIENT8W8T17847W1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48106-115548106-1155-5, 48106-1155-6, 48106-1155-1, 48106-1155-2, 48106-1155-3, 48106-1155-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
LACTIC ACID33X04XA5ATACTIB
UREA8W8T17847WIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 7 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
UREAUREA8W8T17847WINSERT / VAGINAL50 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WCREAM / VAGINAL0.64 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, EXTENDED RELEASE / ORAL0.01 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, COATED / ORAL0.02 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WSYSTEM / TOPICAL840 mgExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WDOUCHE / VAGINAL8 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
UREAUREA8W8T17847WTABLET, EFFERVESCENT / ORAL60 mgExact identifier — unii candidate
7 equally ranked IID candidates

Reported adverse events (FAERS/openFDA)#

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