Label: HC-PRE - pre-dip additive liquid
- NDC Code(s): 86006-0001-1, 86006-0001-2
- Packager: HydroClean
- 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 July 1, 2013
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- INDICATIONS & USAGE
Cleaning, foaming, skin conditioning
For use with HydroClean system
Mixed solution to be used within 72 hours
Use in a well ventilated area
Do not return unused product to original container
For Manufacturing Use OnlyClose
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 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.
PRECAUTION: Avoid eye and skin contact. Moderately irritating to the eyes. Contact with this product may cause severe eye damage. Contact with skin may cause
irritation. May cause irritation of respiratory tract.
STORAGE: Store closed container in a cool, dry, well ventilated area. If product becomes frozen, thaw and mix well before use.
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- PRINCIPAL DISPLAY PANEL
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- INGREDIENTS AND APPEARANCE
pre-dip additive liquid
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:86006-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MYRISTAMINE OXIDE (UNII: J086PM3RRT) (MYRISTAMINE OXIDE - UNII:J086PM3RRT) MYRISTAMINE OXIDE 300 g in 1 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:86006-0001-2 56.8 L in 1 DRUM 2 NDC:86006-0001-1 18.9 L in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2013 Labeler - HydroClean (079165967) Registrant - HydroClean (079165967)