HC-PRE- pre-dip additive liquid

HC-PRE by

Drug Labeling and Warnings

HC-PRE by is a Animal medication manufactured, distributed, or labeled by BouMatic, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

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

PRECAUTIONS

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

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

HC-PRE 
pre-dip additive liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-1200
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: 48106-1200-2	56.8 L in 1 DRUM
2	NDC: 48106-1200-1	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 - BouMatic, LLC (124727400)

Registrant - BouMatic, LLC (124727400)