NDC | 48106-2020-1, 48106-2020-2, 48106-2020-3, 48106-2020-4 |
Set ID | 39275d5d-7af9-4153-b321-20130e9dc397 |
Category | OTC ANIMAL DRUG LABEL |
Packager | BouMatic, LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
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WARNINGS AND PRECAUTIONS
CAUTION
KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE
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.
PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals except as directed.
STORAGE: Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix well before use.
SEE MATERIAL SAFETY DATA SHEET
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INDICATIONS & USAGE
OxyPre-RBT
HYDROGEN PEROXIDE TEAT DIP CONCENTRATE
Helps reduce the spread of organisms which may cause Mastitis
USE DIRECTIONS
NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
Do not use in concentrated form.
Must dilute prior to use.
To obtain a 1.0% hydrogen peroxide solution, 0.5% Lactic Acid and 2% emollients, add 1 part OxyPre-RBT to 9 parts water and mix thoroughly.
Active Ingredient (hydrogen peroxide 10%, Lactic Acid 5%)
Emollients (Sorbitol, Glycerin) 20%
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OXYPRE-RBT
hydrogen peroxide teat dip concentrate liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-2020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE 100 g in 1 L LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT) LACTIC ACID 50 g in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48106-2020-1 19 L in 1 DRUM 2 NDC:48106-2020-2 56.8 L in 1 DRUM 3 NDC:48106-2020-3 208 L in 1 DRUM 4 NDC:48106-2020-4 1041 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/08/2016 Labeler - BouMatic, LLC (124727400) Registrant - BouMatic, LLC (124727400) Establishment Name Address ID/FEI Business Operations Boumatic 080073197 manufacture, api manufacture