VISCO SHIELD  LUBRICANT- hypromellose 2208 (15000 mpa.s) solution/ drops 
OASIS Medical, 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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VISCO SHIELD®
Ophthalmic Lubricant Drops

Drug Facts

Active Ingredients

Hypromellose (1.7%)

Purpose

Ophthalmic lubricant

Uses

Warnings

Stop use and ask a doctor if

  • You experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours, discontinue use and consult a doctor
  • If solution changes color or becomes cloudy, do not use

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

Directions

Questions, or comments

(800) 631-7180 or (909) 305-5400 or log onto www.oasistears.com

Other information

Inactive Ingredients

Calcium chloride dihydrate, hydrochloric acid1, magnesium chloride hexahydrate, potassium chloride, purified water, sodium acetate trihydrate, sodium chloride, sodium citrate dihydrate, and sodium hydroxide1


1
May contain one or more of these ingredients for pH adjustment

PRINCIPAL DISPLAY PANEL - 2 ml Syringe Carton

VISCO SHIELD®
Topical Drops

Ophthalmic
Lubricant Drops

CONTAINS: 6 Pouches, each Pouch containing
1 Single Use Syringe, 0.07 fl oz (2 ml)
1 Single Use Applicator Tip

OASIS®

OASIS® Medical, Glendora CA 91741 USA
© 2014 OASIS Medical
P940 3/2014

Certain manufacturing operations have been performed by other firms

Principal Display Panel - 2 ml Syringe Carton
VISCO SHIELD   LUBRICANT
hypromellose 2208 (15000 mpa.s) solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42126-5200
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPROMELLOSE 2208 (15000 MPA.S) (UNII: Z78RG6M2N2) (HYPROMELLOSE 2208 (15000 MPA.S) - UNII:Z78RG6M2N2) HYPROMELLOSE 2208 (15000 MPA.S)17 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM ACETATE (UNII: 4550K0SC9B)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:42126-5200-06 in 1 CARTON06/16/2014
11 in 1 POUCH
12 mL in 1 SYRINGE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34906/16/2014
Labeler - OASIS Medical, Inc. (194121018)
Establishment
NameAddressID/FEIBusiness Operations
OASIS Medical, Inc.194121018MANUFACTURE(42126-5200)

Revised: 2/2018
Document Id: b0439dd7-d670-4783-b794-721a157b9c44
Set id: 72d22610-d8ab-4f24-b304-8b013430a7d7
Version: 4
Effective Time: 20180202
 
OASIS Medical, Inc.