MINIDROPS- lubricant eye drops liquid

MINIDROPS by

Drug Labeling and Warnings

MINIDROPS by is a Otc medication manufactured, distributed, or labeled by Optics Laboratory, Inc, Taiwan Biotech. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS SECTION

POVIDONE  0.6%

POLYVINYL ALCOHOL  1.4%

PURPOSE SECTION

EYE LUBRICANT

KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

INDICATIONS AND USE SECTION

USES FOR TEMPORARY RELIEF OF BURNING AND IRRITATION DUE TO DRYNESS OF THE EYE

FOR USE AS A PROTECTANT AGAINST FURTHER IRRITATION OR TO RELIEVE DRYNESS OF THE EYE

WARNINGS SECTION

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

IF YOU EXPERIENCE EYE PAIN, CHANGES IN VISION, CONTINUED REDNESS OR IRRITATION OF THE EYE, OR IF THE CONDITIONS WORSENS OR PERSISTS FOR MORE THAN 72 HOURS, DISCONTINUE USE AND CONSULT A DOCTOR. IF SOLUTION CHANGES COLOR OR BECOMES CLOUDY, DO NOT USE

OTHER INFORMATION  STORE AT ROOM TEMPERATURE 15-30 DEGREES C (59-86 DEGREES F)

DOSAGE AND ADMINISTRATION SECTION

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.

INACTIVE INGREDIENTS SECTION

SODIUM CHLORIDE, WATER (PURIFIED)

QUESTIONS SECTION

QUESTIONS OR COMMENTS? 800-968-6788

PACKAGE LABEL

MINIDROPS LUBRICANT EYE DROPS DROPPER

INDIVIDUAL PACKAGE TO AVOID CROSS-CONTAMINATION FROM REPEATED USE

COMPACT MINI-SIZE EASY TO CARRY OPTICS MANUFACTURED FOR OPTICS LABORATORY INC.EL MONTE, CA 91731 USA MADE IN TAIWAN

STERILE PRESERVATIVE FREE USE ONLY IF SINGLE-USE DROPPER IS INTACT  USE AS A PROTECTANT AGAINST FURTHER IRRITATION OR TO RELIEVE DRYNESS OF THE EYE  PRESERVATIVE-FREE FORMULA SAFE FOR DAILY USE  SINGLE-USE DROPPERS, CONVENIENT TO USE AND CARRY

MINIDROPS AND OPTIC LABORATORY ARE TRADEMARKS OF OPTIC LABORATORY INC

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INGREDIENTS AND APPEARANCE

MINIDROPS 
lubricant eye drops liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64108-212
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E)	POVIDONE, UNSPECIFIED	6.0 mg  in 1 mL
POLYVINYL ALCOHOL (UNII: 532B59J990) (POLYVINYL ALCOHOL - UNII:532B59J990)	POLYVINYL ALCOHOL	14.0 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	.9 mg  in 1 mL
WATER (UNII: 059QF0KO0R)	97.1 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64108-212-13	5 in 1 BOX	04/01/1991
1	NDC: 64108-212-10	0.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2	NDC: 64108-212-12	30 in 1 BOX	04/01/1991
2	NDC: 64108-212-10	0.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
3	NDC: 64108-212-65	65 in 1 BOX	04/01/1991
3	NDC: 64108-212-10	0.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	04/01/1991

Labeler - Optics Laboratory, Inc (018503552)

Registrant - Optics Laboratory, Inc (018503552)