REFILL 6- alcohol, water 
CMC Group, Inc.

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Refill 6

Drug Facts - Hand Sanitizer

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

Warnings

Flammable, keep away from fire or flameFor external use only.

Do not use

  • in the eyes.

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach children.

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

Directions

Other information

Store at 15° to 25°C (59° to 77°F)

Inactive ingredients

Carbomer, propylene glycol, purified water, titanium dioxide

Drug Facts - Eye Wash

Active ingredient

Purified Water 99.1%

Purpose

Eyewash

Use

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

Warnings

For external use only.

Do not use

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 • obtain immediate medical treatment for all open wounds in or near the eyes

Stop use and ask a doctor if

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

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

• not for use as contact lens solution

• use before expiration date marked on the bottle

• store at room temperature, 5° to 35°C (41° to 95°F)

Inactive ingredients

Benzalkonium chloride, sodium chloride

Hand Sanitizer (49687-0015-0) Labeling:

Hand sanitizer

Eye Wash (50814-010-01) Labeling:

Eye wash

Refill 6 (49687-0019-0) Labeling:

Refill 6

REFILL 6 
alcohol, water kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49687-0019
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49687-0019-01 in 1 KIT08/10/2016
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 16 BOTTLE 5.4 g
Part 21 TUBE 30 mL
Part 1 of 2
HAND SANITIZER 
alcohol gel
Product Information
Item Code (Source)NDC:49687-0015
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49687-0015-06 in 1 KIT
10.9 g in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)08/10/2016
Part 2 of 2
EYE WASH 
water solution
Product Information
Item Code (Source)NDC:49687-0010
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER991 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49687-0010-11 in 1 BOX
130 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01808/10/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00308/10/2016
Labeler - CMC Group, Inc. (117201448)

Revised: 1/2025
Document Id: 2ba1a752-8549-47e2-e063-6394a90a54d5
Set id: 7849ae59-5484-4b86-a0b9-ec9b93d9afe0
Version: 11
Effective Time: 20250113
 
CMC Group, Inc.