MINIDROPS- lubricant eye drops liquid 
Optics Laboratory, Inc

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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

MiniDrops plastic sleeve v5

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MiniDrops plastic sleeve v5

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MINIDROPS 
lubricant eye drops liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64108-212
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE, UNSPECIFIED6.0 mg  in 1 mL
POLYVINYL ALCOHOL (UNII: 532B59J990) (POLYVINYL ALCOHOL - UNII:532B59J990) POLYVINYL ALCOHOL14.0 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) .9 mg  in 1 mL
WATER (UNII: 059QF0KO0R) 97.1 mg  in 1 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64108-212-135 in 1 BOX04/01/1991
1NDC:64108-212-100.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
2NDC:64108-212-1230 in 1 BOX04/01/1991
2NDC:64108-212-100.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
3NDC:64108-212-6565 in 1 BOX04/01/1991
3NDC:64108-212-100.5 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01804/01/1991
Labeler - Optics Laboratory, Inc (018503552)
Registrant - Optics Laboratory, Inc (018503552)
Establishment
NameAddressID/FEIBusiness Operations
Taiwan Biotech656127933manufacture(64108-212)

Revised: 10/2023
Document Id: dbc3f516-cb64-4ca9-971e-677816181bd0
Set id: c13c5f91-50df-471c-a7c9-1747a2ac1250
Version: 6
Effective Time: 20231030
 
Optics Laboratory, Inc