DROPTICS DRY EYE RELIEF- carboxymethylcellulose sodium,glycerin,polysorbate 80 liquid

Droptics Dry Eye Relief by

Drug Labeling and Warnings

Droptics Dry Eye Relief by is a Otc medication manufactured, distributed, or labeled by Droptics LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Carboxymethylcellulose sodium 0.5%
Glycerin 1%
Polysorbate 80 0.5%

Purpose

Lubricant

Uses

For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun
For use as a protectant against further irritation

Warnings

For external use only
Do not use if solution changes color
When using this product
Do not touch tip of the container to any surface to avoid contamination
Replace cap after each use
Stop use and ask a doctor if
If you feel eye pain
Changes in vision occur
Redness or irritation of the eye lasts
Condition worsens 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

KEEP OUT OF REACH OF CHILDREN

Directions

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

• Tightly screw on cap to seal after use.

Other information

Store at 20 - 25°C (68 -77°F)

Inactive ingredients

L-arginine (amino acid), boric acid, cyanocobalamin (Vitamin B12), L-leucine (amino acid), potassium chloride, purified water, pyridoxine hydrochloride (Vitamin B6), sodium chloride, sodium citrate, stabilized oxychloro complex (as a preservative), taurine (amino acid), tocopherol acetate (Vitamin E), trehalose, sodium hydroxide and/or hydrochloric acid (as needed to adjust pH)

Product label

INGREDIENTS AND APPEARANCE

DROPTICS DRY EYE RELIEF 
carboxymethylcellulose sodium,glycerin,polysorbate 80 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85211-002
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	0.5 g  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 100 mL
POLYSORBATE 80 (UNII: 6OZP39ZG8H) (PEG-20 SORBITAN OLEATE - UNII:6OZP39ZG8H)	POLYSORBATE 80	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ARGININE (UNII: 94ZLA3W45F)
BORIC ACID (UNII: R57ZHV85D4)
CYANOCOBALAMIN (UNII: P6YC3EG204)
LEUCINE (UNII: GMW67QNF9C)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM CHLORITE (UNII: G538EBV4VF)
TAURINE (UNII: 1EQV5MLY3D)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TREHALOSE (UNII: B8WCK70T7I)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROCHLORIC ACID (UNII: QTT17582CB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85211-002-01	1 in 1 CARTON	02/01/2025
1		5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	02/01/2025

Labeler - Droptics LLC (119445348)