Moderate lubricating drops by Velocity Pharma LLC

Moderate lubricating drops by

Drug Labeling and Warnings

Moderate lubricating drops by is a Otc medication manufactured, distributed, or labeled by Velocity Pharma LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MODERATE LUBRICATING DROPS CVS HEALTH- polyethylene glycol 400 solution/ drops 
Velocity Pharma LLC

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OTC - ACTIVE INGREDIENT SECTION

Polyethylene Glycol 400 0.25%

Purpose

Eye lubricant

Uses

• For the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun.
• May be used as a protectant against further irritation.

WARNINGS

• For external use only.
• To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
• Do not use if solution changes color or becomes cloudy.

Stop use and ask 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

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

Other Information

Discard 30 days after opening

RETAIN THIS CARTON FOR FUTURE REFERENCE.

INACTIVE INGREDIENT SECTION

Boric acid, calcium chloride, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium chlorite (OcuPure ® Brand) as a preservative; Sodium Hyaluronate.

Principal Display Panel - 15 mL Bottle Carton

MODERATE LUBRICATING DROPS  CVS HEALTH
polyethylene glycol 400 solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76168-711
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	2.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CHLORITE (UNII: G538EBV4VF)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76168-711-15	1 in 1 CARTON	06/21/2022	10/25/2023
1		15 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	06/21/2022	10/25/2023

Labeler - Velocity Pharma LLC (962198409)

Revised: 1/2024

Document Id: 0fa853a8-61a8-5e6d-e063-6294a90a38ee

34390-5

Set id: e2016198-48ce-9cbc-e053-2995a90ac47d

Version: 2

Effective Time: 20240123