X12 Pre-Post Activator Concentrate

Manufacturer
BOUMATIC, LLC | Knapp Manufacturing, Inc.
Effective date
2023-03-10
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:41:55

Label at a glance#

ProductX12 Pre-Post Activator Concentrate
Active ingredientLACTIC ACID
Label structure6 sections

Dosage and administration

NOT FOR HUMAN USE FOR EXTERNAL USE ONLY Do not mix with any chemicals other than X12 PRE-POST BASE. In a well-ventilated area, mix 1 part X12 PRE-POST ACTIVATOR and 1 part X12 PRE-POST BASE with 2 parts water. Do not mix more product than will be used in 24-hours.

Storage and handling

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

Label contents#

Full prescribing information#

Claim of effectiveness.

SUMMARY OF SAFETY AND EFFECTIVENESS

Helps reduce the spread of organisms
which may cause Mastitis

Use Directions

INSTRUCTIONS FOR USE SECTION

NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
Do not mix with any chemicals other than
X12 PRE-POST BASE.
In a well-ventilated area, mix 1 part X12
PRE-POST ACTIVATOR and 1 part X12
PRE-POST BASE with 2 parts water. Do
not mix more product than will be used
in 24-hours.

First Aid

SAFE HANDLING WARNING SECTION

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.

Precautions & Hazards

GENERAL PRECAUTIONS SECTION

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

General Storage

STORAGE AND HANDLING SECTION

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

label

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
48106-2048-1X12 Pre-Post Activator Concentrate3914 g in 1 PACKAGELIQUID39141
48106-2048-2X12 Pre-Post Activator Concentrate19570 g in 1 PACKAGELIQUID195701
48106-2048-3X12 Pre-Post Activator Concentrate58710 g in 1 PACKAGELIQUID587101
48106-2048-4X12 Pre-Post Activator Concentrate117421 g in 1 PACKAGELIQUID1174211
48106-2048-5X12 Pre-Post Activator Concentrate215271 g in 1 PACKAGELIQUID2152711
48106-2048-6X12 Pre-Post Activator Concentrate1076359 g in 1 PACKAGELIQUID10763591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48106-2048X12 PRE-POST ACTIVATOR CONCENTRATE (CHLORINE DIOXIDE TEAT DIP) LIQUID [BOUMATIC, LLC]16 package rows20230312_ae39aa36-145d-45b7-b43e-0db63f9d64e8.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48106-204848106-2048-1, 48106-2048-2, 48106-2048-3, 48106-2048-4, 48106-2048-5, 48106-2048-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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