HYPROMELLOSE EYE DROPS 0.7% for solution

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35) (HYPROMELLOSE 2910 (4000 MPA.S) - UNII:RN3152OP35)

Available from:

Aurolab

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Therapeutic indications:

- For use as a lubricant to prevent further irritation or to relieve dryness of the eye - If you are sensitive to any ingredient in this product - If solution changes color or becomes cloudy For use as a lubricant to prevent further irritaion or to relieve dryness of the eye

Authorization status:

OTC monograph final

Summary of Product characteristics

HYPROMELLOSE EYE DROPS 0.7%- HYPROMELLOSE EYE DROPS 0.7% FOR SOLUTION
AUROLAB
_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._
----------
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: [e-mail]
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
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)
WAT