HYPROMELLOSE EYE DROPS 0.7% for solution

Hypromellose Eye Drops 0.7% by

Drug Labeling and Warnings

Hypromellose Eye Drops 0.7% by is a Otc medication manufactured, distributed, or labeled by Aurolab. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Hypromellose 0.7% BP w/v

DIRECTIONS FOR USE

• lnstill 1or 2 drops in the affected eye, as needed

INACTIVE INGREDIENT

1. Benzalkonium Chloride
2. Borax
3. Boric acid
4. EDTA disodium salt
5. Potassium chloride
6. Purified water
7. Sodiumchloride

Tamper Protection

• For your protection a tamper evident ring is attached to the bottlecap
• Upon opening, this will separate from the cap and can be discarded
• Use only if this ring is present and attached when the bottle is first opened

USE

• For use as a lubricant to prevent further irritation or to relieve dryness of the eye

Questions

Call: 1-800-103-7321

Email: info@aurolab.com

Web: www.aurolab.com

KEEP OUT OF REACH OF CHILDREN

• If swallowed, get medical help or contact a poison control center right away

ASK DOCTOR

• If you experience eye pain
• Change in vision
• Continued redness(or) irritation of the eye
• Condition worsens or persists for more than 72 hours

DO NOT USE

• If you are sensitive to any ingredient in this product
• If solution changes color or becomes cloudy

Dosage

Instill 1 or 2 drops in the affected eyes as needed

Warnings

For External Use Only

Indications and Usage

For use as a lubricant to prevent further irritaion or to relieve dryness of the eye

Eye Lubricant

Eye Lubricant

CARTON LABEL

INGREDIENTS AND APPEARANCE

HYPROMELLOSE EYE DROPS 0.7% 
hypromellose eye drops 0.7% for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 16030-101
Route of Administration	TOPICAL

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)	7 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM BORATE (UNII: 91MBZ8H3QO)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 16030-101-10	10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	09/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	09/01/2022

Labeler - Aurolab (677319965)

Establishment
Name	Address	ID/FEI	Business Operations
Aurolab		677319965	manufacture(16030-101)