Ice Block

Manufacturer
BouMatic, LLC
Effective date
2012-01-01
Label type
OTC ANIMAL DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:39:30

Label at a glance#

ProductIce Block
Active ingredientSODIUM CAPRYLATE
Label structure3 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

ULTRA HIGH EMOLLIENT TEAT DIP
THAT HELPS PREVENT FROST BITE

Helps reduce the spread of organisms
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%)

PRECAUTIONS SECTION

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 occurs: 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blank LabelBlank Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48106-1135-1Ice Block3.8 L in 1 DRUMLIQUID3.82
48106-1135-2Ice Block18.9 L in 1 DRUMLIQUID18.92
48106-1135-3Ice Block56.8 L in 1 DRUMLIQUID56.82
48106-1135-4Ice Block114 L in 1 DRUMLIQUID1142
48106-1135-5Ice Block208 L in 1 DRUMLIQUID2082
48106-1135-6Ice Block1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID10402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48106-1135ICE BLOCK (SODIUM CAPRYLATE) LIQUID [BOUMATIC, LLC]26 package rows20120531_fd7162a1-5b9b-4bae-a031-63ee05a84ab5.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM CAPRYLATEACTIVE INGREDIENT9XTM81VK2B2
OCTANOIC ACIDACTIVE MOIETYOBL58JN0252

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48106-113548106-1135-1, 48106-1135-2, 48106-1135-3, 48106-1135-4, 48106-1135-5, 48106-1135-6

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CAPRYLATE9XTM81VK2BACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.