Label: EDX-505- iodine liquid
- NDC Code(s): 63927-4162-1, 63927-4162-2, 63927-4162-3
- Packager: ProActive Solutions USA, 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.
Updated November 9, 2023
If you are a consumer or patient please visit this version.
EDX-505™ is a sanitizing iodine teat dip to aid in the prevention of the spread of
mastitis causing organisms.
Use full strength.
Pre-Dipping: Just before milking, make sure the teats are clean and dry. Dip each
teat in undiluted EDX-505™. Allow 5-30 seconds of contact time. Dry with a single
service towel and attach milker units.
Post-Dipping: Immediately after removing inflations, dip each teat in undiluted
EDX-505™. Allow teat to air dry. Do not wipe.
Replace the solution if it becomes visibly dirty.
May be harmful if swallowed. May cause eye irritation.
Do not eat, drink or smoke while using this product. Wear protective clothing, and eye and
Hazards not otherwise classified: None Known
General Advice: May cause eye irritation with corneal injury and result in impairment
External: If irritation occurs, flush with plenty of cool, running water for at least 15 minutes
while removing contaminated clothing and shoes. Wash clothing before reuse.
Eyes: Immediately flush with plenty of cool, running water. Remove contact lenses; then
continue flushing for at least 15 minutes, holding eyelids apart.
Internal: Call a physician immediately. If swallowed, do not induce vomiting. Rinse mouth,
then immediately drink one or two large glasses of water or milk. Never give anything by
mouth to an unconscious person.
Inhalation of vapors: Should not occur with proper use of this product.
Most important symptoms/effects, acute and delayed: None known
Immediate medical attention and special treatment needed, if any: None known
INGREDIENTS AND APPEARANCE
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:63927-4162 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 0.5 kg in 100 kg Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63927-4162-1 57.14 kg in 1 DRUM 2 NDC:63927-4162-2 209.11 kg in 1 DRUM 3 NDC:63927-4162-3 1047.60 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/21/2010 Labeler - ProActive Solutions USA, LLC (029368225) Registrant - ProActive Solutions USA, LLC (029368225) Establishment Name Address ID/FEI Business Operations ProActive Solutions USA, LLC 029368225 api manufacture, manufacture, pack, repack, label