GENTEAL TEARS (MILD) - dextran 70 and hypromellose 2910 solution/ drops 
A-S Medication Solutions

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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Drug Facts

Active IngredientsPurpose
Dextran 70 0.1%Lubricant
Hypromellose 2910 0.3%Lubricant

Uses

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if you experience any of the following:

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients:

POLYQUAD* (polyquaternium-1) 0.001% preservative, potassium chloride, purified water, sodium borate and sodium chloride. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.

HOW SUPPLIED

Product: 50090-2352

NDC: 50090-2352-0 15 mL in a BOTTLE, DROPPER / 1 in a CARTON

Questions?

In the U.S. call 1-800-757-9195
(Mon-Fri 9AM-5PM CST)
alcon.medinfo@alcon.com

dextran 70 and hypromellose 2910

Label Image
GENTEAL TEARS (MILD)  
dextran 70 and hypromellose 2910 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50090-2352(NDC:0065-0418)
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 701 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
Polidronium Chloride (UNII: 6716Z5YR3G)  
Potassium Chloride (UNII: 660YQ98I10)  
Water (UNII: 059QF0KO0R)  
Sodium Borate (UNII: 91MBZ8H3QO)  
Sodium Chloride (UNII: 451W47IQ8X)  
Hydrochloric Acid (UNII: QTT17582CB)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50090-2352-01 in 1 CARTON04/14/2016
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 finalpart34903/01/2016
Labeler - A-S Medication Solutions (830016429)
Establishment
NameAddressID/FEIBusiness Operations
A-S Medication Solutions830016429RELABEL(50090-2352)

Revised: 1/2020
Document Id: 4a6ec6ac-aea1-4b7a-9936-4c70cb16f49c
Set id: 0b427357-b137-4264-9f62-4adaa8b65499
Version: 7
Effective Time: 20200118
 
A-S Medication Solutions