HEXI-SPRAY- chlorhexidine gluconate liquid

Hexi-Spray by

Drug Labeling and Warnings

Hexi-Spray by is a Animal medication manufactured, distributed, or labeled by ProActive Solutions USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Hexi-Spray

Hexi-Spray™ is a post-milking sanitizing teat spray that aids in the prevention of the
spread of mastitis causing organisms. It’s powerful 0.5% Chlorhexidine Gluconate
concentration assures strong germicidal activity while ample amounts of special skin
emollients keep teats soft and smooth.

Use instructions:

Immediately after removing inflations, spray each teat in undiluted Hexi-Spray™.

Allow the teats to air dry. Do not wipe.

Replace the solution if it becomes visibly dirty.

Keep from freezing. If frozen, thaw completely and shake well before using.

Do not use for cleaning or sanitizing equipment.

Caution:

Hazard statement(s):
May be harmful if swallowed. May cause eye irritation.
Precautionary statement(s):
Do not eat, drink or smoke while using this product. Wear protective clothing, and eye
and face protection.
Hazards not otherwise classified: None Known

First Aid:

External: If irritation occurs, flush with plenty of cool, running water for at least 15
minutes while removing contaminated clothing and shoes. Wash clothing before
reuse.
Eyes: Immediately flush with plenty of cool, running water. Remove contact lenses;
then continue flushing for at least 15 minutes, holding eyelids apart.
Internal: Call a physician immediately. If swallowed, do not induce vomiting. Rinse
mouth, then immediately drink one or two large glasses of water or milk. Never give
anything by mouth to an unconscious person.
Inhalation of vapors: Should not occur with proper use of this product.
Most important symptoms/effects, acute and delayed: None known
Immediate medical attention and special treatment needed, if any: None known

Hexi-Spray

INGREDIENTS AND APPEARANCE

HEXI-SPRAY 
chlorhexidine gluconate liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 63927-4190
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE GLUCONATE	0.5 kg  in 100 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63927-4190-1	15.19 kg in 1 CASE
2	NDC: 63927-4190-2	18.99 kg in 1 JUG
3	NDC: 63927-4190-3	59.97 kg in 1 DRUM
4	NDC: 63927-4190-4	208.90 kg in 1 DRUM
5	NDC: 63927-4190-5	1044.48 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/03/2003

Labeler - ProActive Solutions USA, LLC (029368225)

Registrant - ProActive Solutions USA, LLC (029368225)

Establishment
Name	Address	ID/FEI	Business Operations
ProActive Solutions USA, LLC		029368225	api manufacture, manufacture, pack, relabel