CAREALL LUBRICATING EYE DROPS- dextran, hydroxypropyl methylcellulose solution/ drops 
New World Imports, 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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Dextran (70) (0.1%)

Hydroxypropl Methycellulose (2910) (0.3%)

Lubricant

Keep out of reach of children. If swallowed, get medical help or contact a Poision Control Center right away.

  • For the temporary relief of burning and irritation due to dryness of the eye. For protection against further irritation.
  • For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun.

For external use only.  Do not use: If this solution changes color or becomes cloudy or if you are sensitive to any ingredient in this product.

When using this product

  • remove contact lenses before using.
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye gets worse or lasts more than 72 hours.

If pregnant or breast-feeding, ask a health professional before using.

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

Store at room temperature

Benzalkomium Chloride, Potassium Chloride, Disodium Edetate Hydrate, Sodium Borate, Sodium Chloride, Boric Acid, Purified Water

Distributed by: NWI, Inc. 160 Athens Way. Nashville, TN 37228

(615)329-1906

Label

CAREALL LUBRICATING EYE DROPS 
dextran, hydroxypropyl methylcellulose solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51824-040
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 70.1 mg  in 1 mL
HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (HYPROMELLOSE 2910 (4000 MPA.S) - UNII:RN3152OP35) HYPROMELLOSE 2910 (4000 MPA.S).3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
BORIC ACID (UNII: R57ZHV85D4)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51824-040-0515 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34906/01/201412/01/2020
Labeler - New World Imports, Inc (075372276)

Revised: 10/2020
 
New World Imports, Inc