Label: GEA OXYCIDE- peroxide sanitizing teat dip liquid
- NDC Code(s): 51070-7006-2, 51070-7006-3, 51070-7006-5, 51070-7006-6
- Packager: GEA Farm Technologies, Inc.
- 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 June 6, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- KEEP OUT OF REACH OF CHILDREN
- PRECAUTIONS
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USER SAFETY WARNINGS
FIRST AID:
If in Eyes: Flush with large volumes of water for at least 15 minutes. Call a physician immediately.
If Swallowed: DO NOT induce vomiting. Rinse mouth promptly, then give small amount/glass of water (4-6 oz. child / 10-12 oz. adult). Avoid alcohol. Call a physician immediately. DO NOT give anything by mouth to an unconscious or convulsing person.
If on Skin: Flush with large volumes of water for at least 15 minutes while removing contaminated clothing and shoes. If irritation develops and persists, get medical attention.
Inhalation of Vapors: If breathing difficulty or irritation occurs, remove to fresh air. If symptoms persist, get medical attention.FOR ASSISTANCE WITH MEDICAL EMERGENCY
CALL 1-877-741-1032
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- INDICATIONS & USAGE
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DOSAGE & ADMINISTRATION
DIRECTIONS FOR USE: Use at full strength. Do not dilute.
PRE DIPPING: Before milking, dip, spray, or foam each teat with OxyCide. After 15 to 30 seconds, dry each treat thoroughly with a single service towel. If the udder and teats are heavily soiled, wash with a sanitizing solution and dry before application of OxyCide.
- STORAGE AND HANDLING
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- SPL UNCLASSIFIED SECTION
- SPL UNCLASSIFIED SECTION
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- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GEA OXYCIDE
peroxide sanitizing teat dip liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:51070-7006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE 1 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) C12-16 ALCOHOLS (UNII: S4827SZE3L) UREA (UNII: 8W8T17847W) ASCORBIC ACID (UNII: PQ6CK8PD0R) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Product Characteristics Color yellow (clear yellow liquid) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51070-7006-3 56700 g in 1 DRUM 2 NDC:51070-7006-2 18900 g in 1 JUG 3 NDC:51070-7006-5 208000 g in 1 DRUM 4 NDC:51070-7006-6 945000 g in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2010 Labeler - GEA Farm Technologies, Inc. (018037309) Registrant - GEA Farm Technologies, Inc (018037309) Establishment Name Address ID/FEI Business Operations GEA Farm Technologies, Inc. 018037309 api manufacture, manufacture