GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS: Package Insert and Label Information

GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS- povidone and polyvinyl alcohol, unspecified solution/ drops
AmerisourceBergen

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredients

Polyvinyl alcohol…..0.5%

Povidone……0.6%

Purpose

Eye lubricant

Uses

  • for use as a protectant against further irritation or to relieve dryness of the eye
  • for the temporary relief of discomfort due to minor irritations of the eye, or to exposure to wind or sun

Warnings

For external use only

Do not use this product if solution changes color or becomes cloudy

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

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using. Keep container tightly closed.
  • remove contact lens before using

Keep out of the reach of children. If accidentally swallowed , get medical help or contact a Poison Control Center immediately.

Directions

Instill 1 or 2 drops in the affected eye(s) as needed.

Other information

  • Tamper Evident. Do not use this product if imprinted neckband is missing or broken.
  • RETAIN THISCARTON FOR FUTURE REFERENCE
  • Store at 15°-30°C (59°-86°F)

Inactive ingredients

benzalkonium chloride, dextrose, edetate disodium, potassium chloride, purified water, sodium bicarbonate, sodium chloride, sodium citrate, sodium phosphate dibasic, and sodium phosphate monobasic

carton
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GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS
polyvinyl alcohol, povidone solution/ drops
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:24385-006
Route of Administration INTRAOCULAR DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POVIDONE (POVIDONE) POVIDONE 0.6 g in 100 mL
POLYVINYL ALCOHOL, UNSPECIFIED (POLYVINYL ALCOHOL, UNSPECIFIED) POLYVINYL ALCOHOL, UNSPECIFIED 0.5 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
BENZALKONIUM CHLORIDE
EDETATE DISODIUM (EDETIC ACID)
POTASSIUM CHLORIDE
SODIUM CITRATE
SODIUM PHOSPHATE, DIBASIC
SODIUM PHOSPHATE, MONOBASIC
DEXTROSE
WATER
SODIUM BICARBONATE
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:24385-006-05 15 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part349 01/29/2001
Labeler — AmerisourceBergen (007914906)
Registrant — K.C. Pharmaceuticals, Inc. (174450460)
Establishment
Name Address ID/FEI Operations
K.C. Pharmaceuticals, Inc. 174450460 manufacture (24385-006), pack (24385-006), label (24385-006)

Revised: 01/2020 AmerisourceBergen

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