Ice Block: Product Information

ICE BLOCK — sodium caprylate liquid
BouMatic, LLC

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.

ULTRA HIGH EMOLLIENT TEAT DIP
THAT HELPS PREVENT FROST BITE


which may cause Mastitis
USE DIRECTIONS
NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
USE AT FULL STRENGTH
FOR USE IN COLD WEATHER AS
AN AID IN FROST-BITE PREVENTION
POST-DIPPING: Dip as much of the
surface of each teat as possible immediately
after milking.
Note: If solution in cup becomes visibly
dirty, replenish with a fresh mixture
of this product. Do not return
unused product to original container.
Active Ingredient (Caprylic/Capric
Acid 1%)
Emollients (Propylene Glycol 59%,
Butylene Glycol 20%) CAUTION
KEEP OUT OF REACH OF CHILDREN
NOT FOR HUMAN USE
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 occur s: Move person to fresh air. Contact a physician immediately.
If on skin: Take off contaminated clothing. Rinse skin with soap and water.
If irritation develops and persists, contact a physician.
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 contact. Do not ingest. Do not mix with any chemicals except as directed.
STORAGE: Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix
well before use.SEE MATERIAL SAFETY DATA SHEET

Blank Label
(click image for full-size original)

ICE BLOCK sodium caprylate liquid
Product Information
Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1135
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM CAPRYLATE (OCTANOIC ACID) SODIUM CAPRYLATE 60 mL in 10 L
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:48106-1135-1 3.8 L in 1 DRUM None
2 NDC:48106-1135-2 18.9 L in 1 DRUM None
3 NDC:48106-1135-3 56.8 L in 1 DRUM None
4 NDC:48106-1135-4 114 L in 1 DRUM None
5 NDC:48106-1135-5 208 L in 1 DRUM None
6 NDC:48106-1135-6 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK None
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 Operations
BouMatic, LLC 124727400 manufacture, api manufacture

Revised: 01/2012 BouMatic, LLC

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