PEG-Phen Ultra Lubricant Eye Drops description, usages, side effects, indications, overdosage, supplying and lots more!

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PEG-Phen Ultra Lubricant Eye Drops

Amerisource Bergen
Akorn, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

Polyethylene Glycol 400 0.4%

Propylene Glycol 0.3%

Purpose

Lubricant

Lubricant

Uses

For the temporary relief of burning and irritation due to dryness of the eye.

Warnings

For external use only.

Do not use

  • If this product changes color or becomes cloudy
  • If you are sensitive to any ingredient in this product

When using this product

  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye(s) gets worse, persists or lasts more than 72 hours

Keep out of reach of children.

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

Directions

  • Shake well before using
  • Instill 1 or 2 drops in the affected eye(s) as needed.

Other Information

  • Storage: Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

Inactive Ingredients:

Purified Water, Sorbitol solution, Boric Acid, 2-amino-2-methyl-1-propanol, Hypromellose USP, Sodium Chloride, Potassium Chloride. May contain Hydrochloric Acid and/or Sodium Hydroxide to adjust pH;

Preservative: Benzalkonium Chloride.

Questions or comments? 1-800-579-8327

Principal Display Panel Text for Container Label:

46122-201-92

Good Neighbor Pharmacy Logo ®

Ultra Lubricant

Eye Drops

PEG-Phen Ultra Lubricant Eye Drops

10 mL (0.3 fl oz)

Sterile

Principal Display Panel Text for Carton Label:

46122-201-92

Compare to

Systane® Ultra

active ingredients*

Good Neighbor Pharmacy Logo ®

TWIN PACK

Ultra

Lubricant

Eye Drops

PEG-Phen Ultra

Lubricant Eye Drops

2 – 10 mL bottles

(0.6 fl oz total)

Sterile

PEG-Phen Ultra Lubricant Eye Drops

Polyethylene Glycol 400 and Propylene Glycol SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:46122-201
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
polyethylene glycol 400 Polyethylene Glycol 400 4 mg
propylene glycol Propylene Glycol 3 mg

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
BORIC ACID
Aminomethylpropanol
HYPROMELLOSES
SODIUM CHLORIDE
potassium chloride
HYDROCHLORIC ACID
SODIUM HYDROXIDE
benzalkonium chloride

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 10 in 1 BOTTLE, DROPPER
2 NDC:46122-201-92 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-03-22


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