Ventiva Lubricant Eye Drops by Singular Dreamer dba True Marker

Ventiva Lubricant Eye Drops by

Drug Labeling and Warnings

Ventiva Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Singular Dreamer dba True Marker. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

VENTIVA LUBRICANT EYE DROPS- propylene glycol liquid 
Singular Dreamer dba True Marker

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Active Ingredient

Propylene Glycol 0.7%

Purpose

Lubricant

Uses

For the temporary relief of burning and irritation due to 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 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 doctorif you experience any of the
following:

• eye pain 
• change in vision
• continued redness or irritation of the eye
• condition worsens or persists for 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. Put 1 or 2 drops in the affected eye (s) as needed.

Other Information

store at room temperature.

Inactive Ingredients

Water, Boric Acid, Potassium Chloride, Sorbitol, Glycerin, Hyluronic Acid, Amynomethylpropanol, Benzalhonium Chloride, Sodium Chorlide, Hydrochloric Acid, Sodium Hydroxide

Questions ?

888-811-2634

Product label

VENTIVA LUBRICANT EYE DROPS 
propylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83035-8121
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.7 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BORIC ACID (UNII: R57ZHV85D4)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONIC ACID (UNII: S270N0TRQY)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
BENZETHONIUM CHLORIDE (UNII: PH41D05744)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83035-8121-5	1 in 1 CARTON	10/10/2023	11/18/2024
1		5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 83035-8121-9	3 in 1 CARTON	12/22/2023	11/18/2024
2		5 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 83035-8121-4	1 in 1 CARTON	03/11/2024	11/18/2024
3		10 mL in 1 BOTTLE; 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	10/10/2023	11/18/2024

Labeler - Singular Dreamer dba True Marker (129504103)

Registrant - Singular Dreamer dba True Marker (129504103)

Revised: 11/2024

Document Id: 2733bf99-1242-13f1-e063-6394a90ac64d

34390-5

Set id: 6828dd62-f75d-4ea0-8e6c-a7bf00780093

Version: 6

Effective Time: 20241118