X12 Pre-Post Base Concentrate: Product Information

X12 PRE-POST BASE CONCENTRATE- sodium chlorite liquid
BOUMATIC, 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.

Claim of effectiveness.

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
X12 PRE-POST ACTIVATOR.
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

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

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

General Storage

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

label

X12 PRE-POST BASE CONCENTRATE chlorine dioxide teat dip liquid

Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-2049 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (CHLORITE ION) SODIUM CHLORITE 2 g in 100 g

Inactive Ingredients Ingredient Name Strength XANTHAN GUM WATER

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:48106-2049-1 3914 g in 1 PACKAGE None 2 NDC:48106-2049-2 19570 g in 1 PACKAGE None 3 NDC:48106-2049-3 58710 g in 1 PACKAGE None 4 NDC:48106-2049-4 117421 g in 1 PACKAGE None 5 NDC:48106-2049-5 215271 g in 1 PACKAGE None 6 NDC:48106-2049-6 1076359 g in 1 PACKAGE None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/10/2023

Labeler — BOUMATIC, LLC (124727400)

Establishment
Name	Address	ID/FEI	Operations
BOUMATIC, LLC		124727400	api manufacture

Establishment
Name	Address	ID/FEI	Operations
Knapp Manufacturing, Inc.		063012827	manufacture

Revised: 03/2023 BOUMATIC, LLC