DORAMA DRY AID EYE DROPS- povidone, propylene glycol solution 
Sato Pharmaceutical Co., Ltd.

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Dorama Dry Aid Eye Drops

Active ingredients

Povidone 0.68%

Propylene glycol 0.3%

Purpose

Povidone ............... Lubricant

Propylene glycol .....Lubricant

Uses

Warnings

For external use only

When using this product

To avoid contamination

  • do not touch tip of container to any surface
  • replace cap after each use
  • do not use if solution changes color or becomes cloudy
  • remove contact lenses before using

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eyes lasts
  • condition worsens or lasts 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

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride, edetate disodium, menthol, polysorbate 80, purified water, sodium borate, sodium chloride.

Box label

Box label

DORAMA DRY AID EYE DROPS 
povidone, propylene glycol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-503
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 g  in 100 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE0.68 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
LEVOMENTHOL (UNII: BZ1R15MTK7)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
BORIC ACID (UNII: R57ZHV85D4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49873-503-011 in 1 CARTON01/13/202206/30/2025
115 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 DrugM01801/13/202206/30/2025
Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
Establishment
NameAddressID/FEIBusiness Operations
Sato Pharmaceutical Co., Ltd.715699133manufacture(49873-503) , pack(49873-503) , label(49873-503)

Revised: 4/2024
Document Id: 16af0b0e-aba3-9c6f-e063-6394a90ad5c0
Set id: d58650fd-9c6b-3400-e053-2a95a90a3d4c
Version: 3
Effective Time: 20240417
 
Sato Pharmaceutical Co., Ltd.