Label: ATLAS PREP BASE- chlorine dioxide teat dip liquid
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NDC Code(s):
48106-2052-1,
48106-2052-2,
48106-2052-3,
48106-2052-4, view more48106-2052-5, 48106-2052-6
- Packager: BOUMATIC, LLC
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated March 10, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Claim of effectiveness.
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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
- General Storage
- label
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INGREDIENTS AND APPEARANCE
ATLAS PREP BASE
chlorine dioxide teat dip liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-2052 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 13.2 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48106-2052-1 3914 g in 1 PACKAGE 2 NDC:48106-2052-2 19570 g in 1 PACKAGE 3 NDC:48106-2052-3 58710 g in 1 PACKAGE 4 NDC:48106-2052-4 117421 g in 1 PACKAGE 5 NDC:48106-2052-5 215271 g in 1 PACKAGE 6 NDC:48106-2052-6 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
