SUPREME- chlorhexidine gluconate liquid

Supreme by

Drug Labeling and Warnings

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

Drug Details [pdf]

INDICATIONS & USAGE

Helps reduce the spread of organisms
which may cause Mastitis

USE DIRECTIONS

NOT FOR HUMAN USE

FOR EXTERNAL USE ONLY

USE AT FULL STRENGTH

PRE-DIPPING: Before milking, dip
entire teat with this product. Wipe
teats dry after application using single-
service towels to avoid contamination
of milk.

POST-DIPPING: After milking, dip
entire teat with this product. Allow
to air dry.

Note: If solution in cup becomes visibly
dirty, replenish with a fresh mixture
of this product. Do not return
unused product to original container.

PRECAUTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUPREME 
chlorhexidine gluconate liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-1123
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	54 mL  in 10 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-1123-1	3.8 L in 1 DRUM
2	NDC: 48106-1123-2	18.9 L in 1 DRUM
3	NDC: 48106-1123-3	56.8 L in 1 DRUM
4	NDC: 48106-1123-4	114 L in 1 DRUM
5	NDC: 48106-1123-5	208 L in 1 DRUM
6	NDC: 48106-1123-6	1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

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	Business Operations
BouMatic, LLC		124727400	manufacture, api manufacture