ATLAS PREP BASE- chlorine dioxide teat dip 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.

----------

Atlas Prep Base

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 PREP ACTIVATOR.
In well ventilated area, combine 1 gallon
ATLAS PREP BASE and 54 gallons ATLAS
PREP ACTIVATOR, mix or stir vigorously
for at least one minute. Allow mixture to
react for 15-30 minutes prior to application.
Do not mix more product than can be
used in 1 week.

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

Wash skin/ contaminated clothing thoroughly after handling. Wear protective gloves/
protective clothing/ eye protection/ face protection. Do not breathe vapors, mist or spray. 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

image description

ATLAS PREP BASE 
chlorine dioxide teat dip liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:48106-2052
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE13.2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48106-2052-13914 g in 1 PACKAGE
2NDC:48106-2052-219570 g in 1 PACKAGE
3NDC:48106-2052-358710 g in 1 PACKAGE
4NDC:48106-2052-4117421 g in 1 PACKAGE
5NDC:48106-2052-5215271 g in 1 PACKAGE
6NDC:48106-2052-61076359 g in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/10/2023
Labeler - BOUMATIC, LLC (124727400)
Establishment
NameAddressID/FEIBusiness Operations
BOUMATIC, LLC124727400api manufacture
Establishment
NameAddressID/FEIBusiness Operations
Knapp Manufacturing, Inc.063012827manufacture

Revised: 3/2023
Document Id: dc44aa2f-0c7d-459f-9f86-1f81792e9283
Set id: 6eea023d-33d3-4d19-99d2-629bf85e723b
Version: 1
Effective Time: 20230310
 
BOUMATIC, LLC