GOODSENSE LUBRICANT EYE- polyethylene glycol 400, and propylene glycol solution/ drops 
Geiss, Destin & Dunn, Inc

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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GoodSense Lubricant Eye Drops 30 ct. NBE Systane 5474 (2018)

Active ingredients Purposes

Polyethylene glycol 400 0.4%........................................Eye lubricant

Propylene glycol 0.3%...................................................Eye lubricant

Use

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

aminomethylpropanol, boric acid, hydrochlorid acid, hydroxyethyl cellulose, potassium chloride, purified water, sodium chloride, sodium hydroxide, sorbitol

Distributed by:

Geiss, Destin & Dunn, Inc.

Peachtree City, GA 30269

www.valuelabels.com

Made in South Korea

89665

GOODSENSE LUBRICANT EYE 
polyethylene glycol 400, and propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-665
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOLS - UNII:3WJQ0SDW1A) POLYETHYLENE GLYCOL 4004 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SORBITOL (UNII: 506T60A25R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
BORIC ACID (UNII: R57ZHV85D4)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50804-665-3030 in 1 CARTON04/18/2018
10.4 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34904/17/2018
Labeler - Geiss, Destin & Dunn, Inc (076059836)

Revised: 4/2018
Document Id: 6a4f196e-37c4-33f0-e053-2991aa0aa627
Set id: 6936237e-a8f1-8414-e053-2a91aa0a1c87
Version: 3
Effective Time: 20180420
 
Geiss, Destin & Dunn, Inc