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MiniDrops

Taiwan Biotech Co, Ltd
Taiwan Biotech Co, Ltd


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENTS (in each ml)

Polyvinylpyrrolidone 6 mg

Polyvinyl Alcohol 14mg

PURPOSE

PURPOSE      VISCOSITY

PURPOSE 

USE




WARNINGS


DO NOT USE IF THE SINGLE-USE DROPPER IS NOT INTACT.  TO AVOID CONTAMINATION, DO NOT TOUCH TIP OF DROPPER TO ANY SURFACE.  ONCE OPENED, DISCARD.

STOP USE AND ASK A DOCTOR IF

  • THE SOLUTION CHANGES COLOR OR BECOMES CLOUDY
  • EXPERIENCE EYE PAIN
  • CHANGES IN VISION
  • CONDITION WORSENS OR PERSISTS FOR MORE THAN 72 HOURS.

KEEP OUT OF REACH OF CHILDREN

 IF SWALLOWED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

  • TWIST OFF TAB COMPLETELY TO OPEN
  • INSTILL 1 TO 2 DROPS IN THE AFFECTED EYE(S) AS NEEDED
  • DISCARD DROPPER AND DO NOT REUSE

OTHER INFORMATION

STORE AT ROOM TEMPERATURE 15-300 C (59-860 F)

INACTIVE INGREDIENT

SODIUM CHLORIDE

QUESTIONS OR COMMENTS?

800-968-6788









MiniDrops



MiniDrops


MiniDrops





MiniDrops

Lubricant eye drops LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62622-124
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POVIDONE K30 .6 mL
POLYVINYL ALCOHOL 1.4 mL

Inactive Ingredients

Ingredient Name Strength
SODIUM CHLORIDE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62622-124-26 0.5 in 1 VIAL, SINGLE-USE
2 NDC:62622-124-26 0.5 in 1 VIAL, SINGLE-USE
3 NDC:62622-124-24 30 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 1991-04-01


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Be sure to consult your doctor before taking any medication!
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