Eye Drops AC description, usages, side effects, indications, overdosage, supplying and lots more!

Eye Drops AC

KC Pharmaceuticals, Inc.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Tetrahydrozoline HCl 0.05%

Zinc sulfate 0.25%

Purpose

Tetrahydrozoline HCl - Redness reliever

Zinc sulfate - Astringent

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

  • for temporary relief of discomfort and redness of the eye due to minor eye irritations

Warnings

For external use only

Ask a doctor before use if you have narrow angle glaucoma

When using this product

  • pupils may become enlarged temporarily
  • to avoid contamination, do not touch tip of container to any surface.  Replace cap after using.
  • if solution changes color or becomes cloudy, do not use
  • overuse may produce increased redness of the eye
  • remove contact lens before using

Stop use and ask a doctor if you experience

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours

Directions

Instill 1 or 2 drops in the affected eye(s) up to four times daily.

Inactive Ingredients

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium chloride, and sodium citrate

Other information

  • Tamper Evident.  Do not use this product if imprinted neckband is missing or broken.
  • RETAIN THIS CARTON FOR FUTURE REFERENCE
  • Store at 15o - 30oC (59o - 86oF)

If pregnant or breast-feeding,

ask a health professional before use.

Principal Display Panel

EDAC

Principal Display Panel

Eye Drops AC

Tetrahydrozoline hydrochloride, Zinc sulfate SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55651-024
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE 0.5 mg
ZINC SULFATE 2.5 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
BORIC ACID
EDETATE DISODIUM
water
SODIUM CHLORIDE
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:55651-024-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2003-10-23


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Be sure to consult your doctor before taking any medication!
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