THERATEARS LUBRICANT- carboxymethylcellulose sodium solution/ drops 
MEDTECH PRODUCTS INC

----------

TheraTears MD 58790-001

Drug Facts

Active ingredient

Sodium carboxy-
methylcellulose 0.25%

Purpose

Eye lubricant

Uses

Warnings

For external use only

Do not use

  • If solution changes color or becomes cloudy.

Stop use and ask a doctor if

  • You experience eye pain, changes in vision, continued redness or irritation.
  • 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 immediately.

Directions

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

Other information

Inactive ingredients

Borate buffers, calcium chloride, Dequest®, magnesium chloride, potassium chloride, sodium bicarbonate, sodium chloride, sodium perborate, sodium phosphate, and water for injection.

Questions or comments?

1-800-579-8327

Principal Display Panel Text for Carton Label:

thera

tears®

LUBRICANT

EYE DROPS

1 FL OZ (30 mL)

Principal Display Panel Text for Carton Label:
thera
tears®
LUBRICANT
EYE DROPS
1 FL OZ (30 mL)

THERATEARS LUBRICANT 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58790-001
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
carboxymethylcellulose sodium (UNII: K679OBS311) (carboxymethylcellulose - UNII:05JZI7B19X) carboxymethylcellulose sodium2.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
boric acid (UNII: R57ZHV85D4)  
sodium perborate (UNII: Y52BK1W96C)  
calcium chloride (UNII: M4I0D6VV5M)  
diethylenetriamine pentamethylene phosphonic acid (UNII: 0Q75589TM3)  
magnesium chloride (UNII: 02F3473H9O)  
potassium chloride (UNII: 660YQ98I10)  
water (UNII: 059QF0KO0R)  
sodium bicarbonate (UNII: 8MDF5V39QO)  
sodium chloride (UNII: 451W47IQ8X)  
sodium phosphate (UNII: SE337SVY37)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58790-001-301 in 1 CARTON07/01/1999
130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:58790-001-151 in 1 CARTON07/01/1999
215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
3NDC:58790-001-312 in 1 CARTON12/01/2020
330 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 DrugM01807/01/1999
Labeler - MEDTECH PRODUCTS INC (114707784)

Revised: 7/2024
Document Id: e6e715f9-b8f6-4479-b63d-a778b1349ce6
Set id: 661d8764-8ae6-4229-9485-867553ee8e16
Version: 9
Effective Time: 20240709
 
MEDTECH PRODUCTS INC