EPH LABS HAND SANITIZER- alcohol gel 
EPH Laboratories

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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EPH Labs Hand Sanitizer

Drug Facts

Active Ingredients

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Inactive Ingredients

Water, Carbomer Triethanolamine, Glycerin,Propylene Glycol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate.

Uses

• To decrease bacteria and germs on skin • Recommended for repeated use.

Directions

• Wet Hands throughly with product and allow to dry without wiping. • For children under 6, use only under adult supervision. • Not recommended for infants.

Warnings

For external use only-hands. Flammable. Keep away from heat and flame.

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Stop use and ask a doctor

if skin irritation develops.

When using this product:

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. • Do not inhale or ingest. • Avoid contact with broken skin.

Other Information

• Do not store above 105˚F
• May discolour some fabrics
• Harmful to wood finishes and plastics.

Package Labeling: 3786ml

Label

Package Labeling: 1L

Label2

Package Labeling: 300ml

Label3

Package Labeling: 500ml

Label4

EPH LABS HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79759-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
TROLAMINE (UNII: 9O3K93S3TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79759-002-013786 mL in 1 BOTTLE; Type 0: Not a Combination Product07/10/2020
2NDC:79759-002-021000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/10/2020
3NDC:79759-002-03300 mL in 1 BOTTLE; Type 0: Not a Combination Product07/10/2020
4NDC:79759-002-04500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/10/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/10/2020
Labeler - EPH Laboratories (099260755)

Revised: 7/2020
Document Id: ab6cc43f-185b-f69e-e053-2995a90ab73d
Set id: 94d4365d-3cac-4572-8a9d-081aa7c372b5
Version: 1
Effective Time: 20200727
 
EPH Laboratories