Minidrops
FDA Label NDC 62622-124

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Taiwan Biotech Co, Ltd for the product Minidrops (NDC 62622-124). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients (in each ml), purpose, use, warnings, keep out of reach of children, directions, other information, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients (In Each Ml)

Polyvinylpyrrolidone 6 mg

Polyvinyl Alcohol 14mg

Purpose

PURPOSE      VISCOSITY

PURPOSE      VISCOSITY

Use

RELIEVES DRY EYES, DISCOMFORT AND MINOR IRRITATION PROTECTS AND SOOTHES EYE TIREDNESS, EYE STRESS

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








Package Label.Principal Display Panel




5pack Box (Minidrops1a)

5pack Box (Minidrops1a)


5pack Box Backpnl (Minidrops1b)

5pack Box Backpnl (Minidrops1b)





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