Label: FORTICEPT UDDER WASH TEAT CLEANSER AND DISINFECTANT- benzalkonium chloride liquid
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NDC Code(s):
72127-0501-0,
72127-0501-1,
72127-0501-2,
72127-0501-3, view more72127-0501-4, 72127-0501-5
- Packager: LIDAN, 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 April 24, 2018
If you are a consumer or patient please visit this version.
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- Active Ingredients
- Inactive Ingredients
- Uses
- Warnings
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Directions for use
FOR USE AS AN UDDER WASH ONLY!
For daily care: use solution diluted in the ratio of 1:4
1 part of the product is added to 4 parts of water.
Periodic use of undiluted product is allowed (in case of severe contamination).
NOTE: Frequent use of undiluted product may cause mild irritation.
NOTE: The laws in some states require that the sanitizing solution remain in contact with the surface for two minutes. Follow the recommendations of your health department.
- Do not use as a teat dip
- Always use fresh solution
- Wet a single paper or cloth towel with wash solution and wash teats to the base of the udder
- Dry teat with disposable paper or cloth towel before milking
- Use fresh solution if wash solution fades noticeably or becomes diluted or soiled
- Storage and handling
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FIRST AID
Eye contact: In case of contact, immediately flush eyes with cool running water.
Remove contact lenses and continue flushing with plenty of water for at least 15 minutes. Get medical attention if irritation persists.
Skin contact: Wash the skin with water and soap. Wash clothing before reuse.
Ingestion: If large quantities of this material are swallowed, call a poison control center immediately.
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INGREDIENTS AND APPEARANCE
FORTICEPT UDDER WASH TEAT CLEANSER AND DISINFECTANT
benzalkonium chloride liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:72127-0501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 13 g in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72127-0501-0 1 L in 1 BOTTLE 2 NDC:72127-0501-1 3.785 L in 1 BOTTLE 3 NDC:72127-0501-2 5 L in 1 BOTTLE 4 NDC:72127-0501-3 10 L in 1 BOTTLE 5 NDC:72127-0501-4 20 L in 1 BOTTLE 6 NDC:72127-0501-5 1000 L in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/15/2018 Labeler - LIDAN, INC. (014456716) Registrant - LIDAN, INC. (014456716) Establishment Name Address ID/FEI Business Operations Cosco International, Inc. 016433141 analysis, manufacture, pack Establishment Name Address ID/FEI Business Operations DISHMAN CARBOGEN AMCIS LIMITED 915628142 api manufacture Establishment Name Address ID/FEI Business Operations Univar USA Inc. 042953927 api manufacture Establishment Name Address ID/FEI Business Operations Pharmex Group LLC 365309015 pack, repack
