HYLATEARS- eye drops liquid

HylaTears by

Drug Labeling and Warnings

HylaTears by is a Otc medication manufactured, distributed, or labeled by Hyalogic LLC, Regulatory Matters Consulting. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

WARNINGS

INACTIVE INGREDIENT

INDICATIONS & USAGE

PURPOSE

HylaTears Updated Box

INGREDIENTS AND APPEARANCE

HYLATEARS 
eye drops liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72094-001
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (HYPROMELLOSE 2910 (4000 MPA.S) - UNII:RN3152OP35)	HYPROMELLOSE 2910 (4000 MPA.S)	3 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)
SODIUM PHOSPHATE LINKAGE (UNII: M895BOC3WI)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72094-001-01	20 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	02/12/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	02/12/2018

Labeler - Hyalogic LLC (026884299)

Registrant - Regulatory Matters Consulting (080711165)