EQUATE DAY AND NIGHT RESTORE TEARS- mineral oil, white petrolatum and carboxymethylcelluose sodium 
Wal-Mart Stores, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Equate Day and Night Restore Tears

Walmart

Equate

Day & Night Restore Tears

15mL & 3.5g

NDC 49035-883-59

Restore PM Lubricant Eye Ointment NDC# 49035-191-50

Drug Facts

Active ingredients

Mineral Oil 42.5% and White Petrolatum 57.3%

Purpose

Lubricant

Uses

Warnings

When using this product

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

Stop use and ask a doctor if

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

If pregnant or breast feeding,

ask a health professional before use. 

Keep this and all drugs out of the reach of children. 

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

Directions

Other information

Inactive ingredients

lanolin alcohols

Walmart

Equate

Day & Night Restore Tears

15mL & 3.5g

NDC 49035-883-59

Restore Tears Lubricant Eye Drops NDC 49035-189-13

Drug Facts

Active ingredients

Carboxymethylcellulose Sodium 0.5%

Purpose

Eye Lubricant

Uses

Warnings

Do not use

  • if this product changes color or becomes cloudy.

When using this product

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

Stop use and ask a doctor if  

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

Keep this and all drugs out of the reach of children.

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

Directions

Other information

Inactive ingredients

Boric Acid, calcium chloride, magnesium chloride, potassium chloride, sodium borate, water for injection. Vanish® (Stabilized Peroxycomplex System as a preservative). May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

PRINCIPAL DISPLAY PANEL

NDC 49035-883-59
Equate
Day & Night
Restore Tears
15mL & 3.5g

PRINCIPAL DISPLAY PANEL
NDC 49035-883-59
Equate
Day & Night 
Restore Tears
15mL & 3.5g

EQUATE DAY AND NIGHT RESTORE TEARS 
mineral oil, white petrolatum and carboxymethylcelluose sodium kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-883
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-883-591 in 1 CARTON; Type 1: Convenience Kit of Co-Package06/01/2018
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE, DROPPER 15 mL
Part 21 TUBE 3.5 g
Part 1 of 2
RESTORE TEARS LUBRICANT EYE 
carboxymethylcellulose sodium solution/ drops
Product Information
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
WATER (UNII: 059QF0KO0R)  
CHLORINE DIOXIDE (UNII: 8061YMS4RM)  
POLIHEXANIDE (UNII: 322U039GMF)  
Other Ingredients
Ingredient KindIngredient NameQuantity
May containHYDROCHLORIC ACID (UNII: QTT17582CB)  
May containSODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34906/01/2018
Part 2 of 2
RESTORE PM LUBRICANT EYE 
mineral oil, petrolatum ointment
Product Information
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MINERAL OIL (UNII: T5L8T28FGP) (MINERAL OIL - UNII:T5L8T28FGP) MINERAL OIL425 mg  in 1 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM573 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
13.5 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34906/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34906/01/2018
Labeler - Wal-Mart Stores, Inc. (051957769)

Revised: 5/2018
Document Id: 35879cd7-117e-4942-96f2-19107b4995bd
Set id: b705b4fb-db66-47f4-810c-f3cda4a2d40f
Version: 3
Effective Time: 20180507
 
Wal-Mart Stores, Inc.