HEB EYE DROPS- glycerin, naphazoline hydrochloride liquid 
H E B

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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HEB Eye Drops

Active ingredients

Glycerin 0.5%

Naphazoline hydrochloride 0.03%

Purpose

Lubricant

Redness reliever

Uses

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

  • To avoid contamination, do not touch tip of container to any surface.
  • Replace cap after using.
  • Overuse may produce increased redness of the eye
  • Pupils may become enlarged temporarily.

Stop use and ask a doctor if

  • you experience eye pain
  • you experience changes in vision
  • you experience 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

Other information

Store at room temperature.

Inactive ingredients

benzalkonium chloride, boric acid, disodium edetate hydrate, sodium borate, water for injection

Package label

carton

package label

carton

HEB EYE DROPS 
glycerin, naphazoline hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-560
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE0.12 mg  in 15 mL
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2.5 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37808-560-022 in 1 BOX12/11/2020
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
2NDC:37808-560-011 in 1 BOX12/11/2020
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 finalpart34912/11/2020
Labeler - H E B (007924756)

Revised: 1/2023
Document Id: f344ff26-4cf6-2f7a-e053-2a95a90abfbf
Set id: b67925c0-8b14-787a-e053-2995a90a79b1
Version: 2
Effective Time: 20230127
 
H E B