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.

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Active Ingredient

Hypromellose 0.7% BP w/v

DIRECTIONS FOR USE

INACTIVE INGREDIENT

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

Tamper Protection

USE

Questions

Call: 1-800-103-7321

Email: info@aurolab.com

Web: www.aurolab.com

KEEP OUT OF REACH OF CHILDREN

ASK DOCTOR

DO NOT USE

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

HPMC

HYPROMELLOSE EYE DROPS 0.7% 
hypromellose eye drops 0.7% for solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16030-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
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 NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:16030-101-1010 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product09/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/01/2022
Labeler - Aurolab (677319965)
Establishment
NameAddressID/FEIBusiness Operations
Aurolab677319965manufacture(16030-101)

Revised: 8/2023
Document Id: 039b83ec-e62a-e1f9-e063-6394a90ae83a
Set id: d35313d0-b190-5fb0-e053-2a95a90a5283
Version: 5
Effective Time: 20230823
 
Aurolab