AEROWASH EYEWASH- eyewash solution liquid 
Aero Healthcare US LLC

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AeroWash Eyewash - eyewash solution

ACTIVE INGREDIENT

Purified water 98.3%

PURPOSE

Eyewash

WARNINGS

For external use only

Do not use

  • if you experience any open wounds in or near the eyes and obtain immediate medical treatment
  • if solution changes color or becomes cloudy

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • do not reuse
  • once opened, discard

Stop use and ask a doctor if you have any of the following

  • changes in vision
  • eye pain
  • condition worsens or persists
  • continued redness or irritation of the eye

Use

For cleansing the eye to help relieve irritation or burning by removing loose foreign material

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

OTHER INFORMATION

INACTIVE INGREDIENTS

boric acid, sodium borate, sodium chloride

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL – 1 FL OZ (30 ML) LABEL

1 oz.

1oz 2

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL – 4 FL OZ (118 ML)

4 OZ

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL – 16 FL OZ (473 ML)

16 OZ

PACKAGE/LABEL PRINCIPAL DISPLAY PANEL – 32 FL OZ (946 ML)

32 OZ.

AEROWASH EYEWASH 
eyewash solution liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55305-115
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER0.983 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55305-115-1030 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product01/01/2020
2NDC:55305-115-11118 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product01/01/2020
3NDC:55305-115-12473 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product01/01/2020
4NDC:55305-115-13946 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product01/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02230501/01/2020
Labeler - Aero Healthcare US LLC (008186174)
Registrant - Aero Healthcare US LLC (008186174)

Revised: 4/2020
Document Id: a477de08-4302-0ee5-e053-2995a90af79d
Set id: a477de08-4301-0ee5-e053-2995a90af79d
Version: 1
Effective Time: 20200429
 
Aero Healthcare US LLC