Label: DERMAPRO- dermal conditioner teat dip solution
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NDC Code(s):
60648-9017-1,
60648-9017-2,
60648-9017-3,
60648-9017-4, view more60648-9017-5, 60648-9017-6, 60648-9017-7
- Packager: Preserve International
- 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 May 21, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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DIRECTIONS FOR USE:
Use at full strength, do not dilute.
APPLICATION:
FOR POST-DIPPING: Dip entire teat in DERMAPRO. Allow to air dry. If solution in cup becomes visibly dirty or cloudy, then replenish with DERMAPRO at full strength.
FOR FRESHENING COWS: Dip teat twice daily for 10 days before calving.
FOR DRY COWS: Dip teat once a day for several days following last milking.
Do not return unused product to original container.
NOTE:
This product does not contain NPE (Nonylphenol Ethoxylate) Surfactant.
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WARNING:
Avoid contamination of food. Avoid contact with eyes. Not for internal use. Not for human use. Wash hands thoroughly after contact with product.
KEEP OUT OF REACH OF CHILDREN
FIRST AID:
INHALATION: No irritation expected. Move the exposed person to fresh air.
EYE CONTACT: Rinse immediately with plenty of water. Contact lenses should be removed.
SKIN CONTACT: No irritation expected. Rinse immediately with plenty of water.
INGESTION: DO NOT INDUCE VOMITING unless advised to do so by a doctor. Never give anything by mouth to an unconscious person.
GET MEDICAL ATTENTION IMMEDIATELY.FOR PRODUCT EMERGENCY CONTACT: Chem-Tel Inc. 1-800-255-3924
- WARNING:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DERMAPRO
dermal conditioner teat dip solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:60648-9017 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAPRYLIC/CAPRIC ACID (UNII: DI775RT244) (CAPRYLIC/CAPRIC ACID - UNII:DI775RT244) CAPRYLIC/CAPRIC ACID 11.15 g in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60648-9017-1 3.78 L in 1 JUG 2 NDC:60648-9017-2 18.9 L in 1 PAIL 3 NDC:60648-9017-3 56.7 L in 1 DRUM 4 NDC:60648-9017-4 113.4 L in 1 DRUM 5 NDC:60648-9017-5 207.9 L in 1 DRUM 6 NDC:60648-9017-6 945 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK 7 NDC:60648-9017-7 1039.5 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 03/18/2019 Labeler - Preserve International (808154199)
