ATLAS BARRIER BASE- chlorine dioxide teat dip liquid

Atlas Barrier Base by

Drug Labeling and Warnings

Atlas Barrier Base 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 other chemicals other
than ATLAS BARRIER ACTIVATOR.
In well ventilated area, mix 1 part ATLAS
BARRIER BASE and 1 part ATLAS BARRIER
ACTIVATOR. Allow mixture to react for 15-
30 minutes prior to application. Do not mix
more product than can be used in 1 week.
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.

First Aid

FIRST AID:
If in eyes: Hold eye open and rinse slowly and gently with water for at least 15 minutes. Remove contact
lenses, if present and easy to do. Continue rinsing. Contact a physician immediately. If swallowed:
Rinse mouth with water. Do not give anything to an unconscious person. Do not induce vomiting. Contact
a physician immediately. If Inhaled: Move person to fresh air. Contact a physician immediately. If
on skin: Immediatly remove contaminated clothing. Rinse skin with water. Use soap if available. Wash
clothes before reuse. 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 SDS, or a poison control center.

Precautions & Hazards

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

ATLAS BARRIER BASE 
chlorine dioxide teat dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2054
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	0.74 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2054-1	3914 g in 1 PACKAGE
2	NDC: 48106-2054-2	19570 g in 1 PACKAGE
3	NDC: 48106-2054-3	58710 g in 1 PACKAGE
4	NDC: 48106-2054-4	117421 g in 1 PACKAGE
5	NDC: 48106-2054-5	215271 g in 1 PACKAGE
6	NDC: 48106-2054-6	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