EYE DROPS- glycerin solution

Eye Drops by

Drug Labeling and Warnings

Eye Drops by is a Otc medication manufactured, distributed, or labeled by Opto-Pharm Pte Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Glycerin.....1.0%

Purpose

Lubricant

Uses

• For use as a lubricant to prevent 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 if

solution changes color or becomes cloudy

When using this product

• to avoid contamination, do not touch tip  of container to any surface
• replace cap after using

Stop use and ask a doctor if

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

Keep out of reach of children

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

Directions

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

Other informations

• store in the refrigerator
• do not freeze
• store in dark, cool place away from sunlight
• once open, discard container and any contents after 30 days
• use before expiration date marked on container
• prior to drop instillation, contact lenses should be removed and reinserted after 10 minutes

Inactive ingredients

boric acid, citric acid, hypromellose, N-acetyl-carnosine, potassium bicarbonate, purified benzyl alcohol, sterile water

Questions

+65-68614801

Principal Display Panel

NDC: 46823-001-05

STERILE LUBRICANT EYE DROPS

2X0.17 fl oz/5 ml vials

(Net 0.34 fl oz/10 ml)

INGREDIENTS AND APPEARANCE

EYE DROPS 
glycerin solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46823-001
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
N-ACETYLCARNOSINE (UNII: 0TPN86OQIF)
POTASSIUM BICARBONATE (UNII: HM5Z15LEBN)
BENZYL ALCOHOL (UNII: LKG8494WBH)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46823-001-05	10 g in 1 VIAL; Type 0: Not a Combination Product	03/06/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	03/06/2017

Labeler - Opto-Pharm Pte Ltd (595239682)

Registrant - Opto-Pharm Pte Ltd (595239682)