CVS Health: Multi- Action Relief Drops

Multi- Action Relief Drops by

Drug Labeling and Warnings

Multi- Action Relief Drops by is a Otc medication manufactured, distributed, or labeled by Velocity Pharma LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MULTI- ACTION RELIEF DROPS- polyvinyl alcohol and povidone and tetrahydrozoline hydrochloride solution/ drops 
Velocity Pharma LLC

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CVS Health: Multi- Action Relief Drops

Drug Facts

Active ingredients

Polyvinyl alcohol 0.5%

Active ingredients

Povidone 0.6%

Purpose

Lubricant

Active ingredient

Tetrahydrozoline hydrochloride 0.05%

Purpose

Redness reliever

Uses

• for the temporary relief of burning & irritation due to dryness of the eye
  
• for use as a protectant against further irritation or to relieve dryness of the eye
  
• relieves redness of the eye due to minor eye irritations

Warnings

For external use only

Do not use if

solution changes color or becomes cloudy.

Ask a doctor before use if you have

narrow angle glaucoma.

When using this product

• to avoid contamination, do not touch tip to any surface
  
• replace cap after using
  
• overuse may produce increased redness of the eye
  
• pupils may become enlarged temporarily

Stop use & 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
  
• symptoms last for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center(1-800-222-1222) right away.

Directions

Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Other information

• store at room temperature
  
• remove contact lenses before using
• retain carton for future reference

Inactive ingredients

benzalkonium chloride, disodium hydrogen phosphate, edetate disodium, mannitol, sodium dihydrogen phosphate dihydrate, potassium chloride, purified water, sodium chloride, sodium citrate.

May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

PRINCIPAL DISPLAY PANEL

MULTI- ACTION RELIEF DROPS 
polyvinyl alcohol and povidone and tetrahydrozoline hydrochloride solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76168-706
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990)	POLYVINYL ALCOHOL, UNSPECIFIED	5 mg  in 1 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E)	POVIDONE	6 mg  in 1 mL
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077)	TETRAHYDROZOLINE HYDROCHLORIDE	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
EDETATE DISODIUM (UNII: 7FLD91C86K)
MANNITOL (UNII: 3OWL53L36A)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76168-706-15	1 in 1 CARTON	03/15/2011	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	03/15/2011	10/25/2023

Labeler - Velocity Pharma LLC (962198409)

Registrant - Velocity Pharma LLC (962198409)

Revised: 1/2024

Document Id: 0fa7eb87-9b66-161f-e063-6294a90a2737

34390-5

Set id: b0c85182-2381-7323-e053-2a95a90a5c52

Version: 5

Effective Time: 20240123