ADVANCED EYE RELIEF/ REDNESS MAXIMUM RELIEF- naphazoline hydrochloride and hypromellose solution/ drops 
Bausch & Lomb Incorporated

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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Drug Facts

Active ingredients

Hypromellose (0.5%)
Naphazoline hydrochloride (0.03%)

Purpose

Lubricant
Redness reliever

Uses

temporary relief of redness and discomfort due to:
minor eye irritations
exposure to wind or sun
dryness of the eye
prevents further irritation

Warnings

For external use only

Do not use

if solution changes color or becomes cloudy

Ask a doctor before use if you have

narrow angle glaucoma

When using this product

do not touch tip of container to any surface to avoid contamination
do not overuse as it may produce increased redness of the eye
pupils may become enlarged temporarily
remove contact lenses before using
replace cap after use

Stop use and ask a doctor if

you experience eye pain, changes in vision, continued redness or irritation of the eye
condition worsens or persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

instill 1 to 2 drops in the affected eye(s) up to four times daily

Other information

store at 15–25 °C (59–77 °F)
keep tightly closed
use before expiration date marked on the carton and bottle

Inactive ingredients

benzalkonium chloride, boric acid, edetate disodium, sodium borate, sodium chloride, water for injection. Hydrochloric acid and/or sodium hydroxide may be used to adjust pH.

Questions or comments?

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Package/Label Principal Display Panel

carton

BAUSCH + LOMB
ADVANCED
Eye Relief®
Maximum
Redness
REDNESS RELIEVER/
LUBRICANT EYE DROPS

Maximum strength redness reliever
Moisturizes and comforts

STERILE 0.5 FL OZ (15 mL)

3843902
AB55411A

ADVANCED EYE RELIEF/ REDNESS MAXIMUM RELIEF 
naphazoline hydrochloride and hypromellose solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-450
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) (HYPROMELLOSE, UNSPECIFIED - UNII:3NXW29V3WO) HYPROMELLOSE, UNSPECIFIED5 mg  in 1 mL
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24208-450-151 in 1 CARTON09/02/2010
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:24208-450-902 in 1 CARTON07/31/202207/31/2022
215 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34909/02/2010
Labeler - Bausch & Lomb Incorporated (196603781)
Establishment
NameAddressID/FEIBusiness Operations
Bausch & Lomb Incorporated079587625MANUFACTURE(24208-450)

Revised: 8/2023
Document Id: 4591fc36-d88f-42d0-bba0-c5e47a4d4278
Set id: 3c11285a-7e86-4b47-b1ee-e7d59858087d
Version: 8
Effective Time: 20230817
 
Bausch & Lomb Incorporated