Sani-Star DermaStar Plus description, usages, side effects, indications, overdosage, supplying and lots more!

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Sani-Star DermaStar Plus

BouMatic, LLC
BouMatic, LLC

Sani-Star DermaStar Plus




FULL PRESCRIBING INFORMATION

Uses

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, foam or spray entire teat with this product. Wipe teats dry after application using single-service towels to avoid contamination of milk.

POST-DIPPING: After milking, spray, foam or 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.

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

Sani-Star DermaStar Plus

Sani-Star DermaStar Plus

IODINE LIQUID

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:48106-1147
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Iodine IODINE 108 mL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:48106-1147-1 3.8 in 1 DRUM
2 NDC:48106-1147-2 18.9 in 1 DRUM
3 NDC:48106-1147-3 56.8 in 1 DRUM
4 NDC:48106-1147-4 114 in 1 DRUM
5 NDC:48106-1147-5 208 in 1 DRUM
6 NDC:48106-1147-6 1040 in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2007-08-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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