Label: ORBIT CLEAN ACTIVATOR- chlorine dioxide teat dip liquid
- NDC Code(s): 43104-2016-1
- Packager: Knapp Manufacturing, Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 22, 2022
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
MIX DIRECTIONS-SURFACE CLEANING: Do not mix with any chemicals other than Orbit-
Clean Base. In a well-ventilated area, mix equal parts Orbit-Clean Base and Orbit-Clean
Activator to 10 parts water (1:1:20). Do not mix more product than will be used in 48 hours.
USE DIRECTIONS-SURFACE CLEANING
1) Remove surface contaminates.
2) Coat surface thoroughly with blended product.
3) Leave on, do not rinse.
FOR TEAT DIP MIX AND USAGE DIRECTIONS, CONTACT YOUR BOUMATIC REPRESENTATIVE. -
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 SDS, or a poison control center. - Precautions & Hazards
- General Storage
- Claim of effectiveness.
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INGREDIENTS AND APPEARANCE
ORBIT CLEAN ACTIVATOR
chlorine dioxide teat dip liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:43104-2016 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT) LACTIC ACID 0.066 kg in 1 kg Inactive Ingredients Ingredient Name Strength SODIUM XYLENESULFONATE (UNII: G4LZF950UR) C8-10 ALCOHOLS (UNII: 6X61I5U3A4) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43104-2016-1 3.92 kg in 1 JUG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/22/2022 Labeler - Knapp Manufacturing, Inc. (063012827) Establishment Name Address ID/FEI Business Operations Knapp Manufacturing, Inc. 063012827 api manufacture Establishment Name Address ID/FEI Business Operations BouMatic, LLC 124727400 manufacture