Label: STEPSEPT CSE-200- phosphoric acid liquid
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NDC Code(s):
48106-1150-1,
48106-1150-2,
48106-1150-3,
48106-1150-4, view more48106-1150-5, 48106-1150-6
- Packager: BouMatic, 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.
Drug Label Information
Updated January 1, 2012
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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INDICATIONS & USAGE
Concentrated hoof bath enhancer
NOT FOR HUMAN USE
DIRECTIONS FOR HOOFBATH SYSTEMS to help prevent Hoof Rot and Hairy Heel Warts
Dilute and mix 0.5 gallon (2 L) of this product with half the normal amount of footbath additive diluted to 50 gallons (190 L) with water. For example: 0.5 gallon (2 L) of this product plus 25 pounds (11 kg) of copper sulfate diluted to 50 gallons (190 L) is equal to or better than 50 pounds (23 kg) of copper sulfate diluted to 50 gallons (190 L). Rinse and clean footbaths when solution becomes excessively contaminated.
RECOMMENDATION: To increase efficacy of StepSept CSE-200, use a cleaning foot bath in conjunction with BouMatic’s StepSept PB-50, a pre-bath hoof cleaner concentrate to help maintain clean treatment solutions.
Active Ingredients (Phosphoric Acid 20%, Third Generation Quaternary Ammonium Chloride 10%)
Inactive Ingredients (Ethanol, Water, FD(and)C Blue No. 1) -
PRECAUTIONS
DANGER
KEEP OUT OF REACH OF CHILDREN
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 immediately with plenty of water for 15-20 minutes. Contact a physician immediately.
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.HAZARD: Corrosive. Contains Phosphoric Acid. Severe eye, skin, and digestive tract irritant. May cause permanent eye damage. Contact with chlorinated compounds liberates toxic gas. Contact with alkalis generates heat.
PRECAUTION: Avoid eye and skin contact. Do not breathe mist or spray. Wear impermeable gloves, safety glasses, rubber boots, rubber apron and face shield. Use only in well-ventilated area. Do not mix with alkaline or chlorinated materials.
STORAGE: Store closed container in a cool, dry location away from sources of heat. If product becomes frozen, thaw and mix well before use.
SEE MATERIAL SAFETY DATA SHEET
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STEPSEPT CSE-200
phosphoric acid liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 1500 mg in 10 L BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 400 mg in 10 L N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) (UNII: G258TFN61X) (N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM (C12-C14) - UNII:85440928RV) N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) 400 mg in 10 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48106-1150-1 3.8 L in 1 DRUM 2 NDC:48106-1150-2 18.9 L in 1 DRUM 3 NDC:48106-1150-3 56.8 L in 1 DRUM 4 NDC:48106-1150-4 114 L in 1 DRUM 5 NDC:48106-1150-5 208 L in 1 DRUM 6 NDC:48106-1150-6 1040 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 08/01/2007 Labeler - BouMatic, LLC (124727400) Registrant - BouMatic, LLC (124727400) Establishment Name Address ID/FEI Business Operations BouMatic, LLC 124727400 manufacture, api manufacture Establishment Name Address ID/FEI Business Operations Knapp Manufacturing 063012827 manufacture, api manufacture
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