Your browser does not support JavaScript! HC-PRE (PRE-DIP ADDITIVE) LIQUID [HYDROCLEAN]

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HC-PRE (pre-dip additive) liquid
[HydroClean]


Category DEA Schedule Marketing Status
OTC ANIMAL DRUG LABEL unapproved drug other
NOTE: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 Sections


Pre-Dip Additive

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 Only

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 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.

SEE MATERIAL SAFETY DATA SHEET

Blank LabelEnter section text here

HC-PRE 
pre-dip additive liquid
Product Information
Product TypeOTC ANIMAL DRUG LABELItem Code (Source)NDC:86006-0001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MYRISTAMINE OXIDE (MYRISTAMINE OXIDE) MYRISTAMINE OXIDE300 g  in 1 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:86006-0001-256.8 L in 1 DRUM
2NDC:86006-0001-118.9 L in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other07/01/2013
Labeler - HydroClean (079165967)
Registrant - HydroClean (079165967)

Revised: 7/2013
 
HydroClean

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