X12 PRE-POST BASE CONCENTRATE- chlorine dioxide teat dip liquid

X12 Pre-Post Base Concentrate by

Drug Labeling and Warnings

X12 Pre-Post Base Concentrate by is a Animal medication manufactured, distributed, or labeled by BOUMATIC, LLC, Knapp Manufacturing, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 mix
well before use.

label

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2049-1	3914 g in 1 PACKAGE
2	NDC: 48106-2049-2	19570 g in 1 PACKAGE
3	NDC: 48106-2049-3	58710 g in 1 PACKAGE
4	NDC: 48106-2049-4	117421 g in 1 PACKAGE
5	NDC: 48106-2049-5	215271 g in 1 PACKAGE
6	NDC: 48106-2049-6	1076359 g in 1 PACKAGE

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	Business Operations
BOUMATIC, LLC		124727400	api manufacture

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