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Natural Balance Tears

Dosage form: solution/ drops
Ingredients: HYPROMELLOSE 2910 (3 MPA.S) 4mg in 1mL
Labeler: Major Pharmaceuticals
NDC code: 0904-5018

Natural Balance Tears Drug Facts

Active ingredient

Hypromellose 0.4%

Purpose

Lubricant

Uses
  • to prevent further irritation

    to relieve dryness of the eye

Warnings

Do not use if solution changes color or becomes cloudy

When using this product  

  • do not touch tip of container to any surface to avoid contamination
  • 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
  • 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
  • instill 1 to 2 drops in the affected eye(s) as needed

Other information
  • store at 15° - 30°C (59° - 86°F)
  • keep tightly closed

Inactive ingredients

dibasic sodium phosphate, edetate disodium, monobasic sodium phosphate,

potassium chloride, sodium chloride, purified water.

Hydrochloric acid and/or sodium hydroxide may be added to adjust pH.

PRESERVATIVE ADDED: benzalkonium chloride 0.01%

Questions ?

Serious side effects associated with use of this product may be reported to 1800-323-0000

©Major Pharmaceuticals

Package/Label Principal Display Panel

NDC 0904-5018-35

MAJOR®

nature balance Tears

Lubricant Eye Drops

Sterile

Relieves Dryness of the Eye

Compare to Active Ingredient in Tears Naturale®*

15 mL (1/2 FL. OZ.)

NATURAL BALANCE TEARS 
hypromellose solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0904-5018
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPROMELLOSE 2910 (3 MPA.S) (HYPROMELLOSES) HYPROMELLOSE 2910 (3 MPA.S)4 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM PHOSPHATE, DIBASIC 
EDETATE DISODIUM 
SODIUM PHOSPHATE, MONOBASIC 
POTASSIUM CHLORIDE 
SODIUM CHLORIDE 
WATER 
BENZALKONIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:0904-5018-3515 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34910/07/2011
Labeler - Major Pharmaceuticals (191427277)
Establishment
NameAddressID/FEIOperations
Bausch & Lomb Incorporated807927397MANUFACTURE

Revised: 12/2011
 
Major Pharmaceuticals

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.