EDDDIES HAND SANITIZER GEL- alcohol 75% gel 
Nutralife Biosciences, 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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Eddie's Gel Hand Sanitizer 8oz Nutralife

Active Ingredient

Alcohol 75%

Purpose

Antiseptic

Uses

To help reduce bacteria on the skin. For use when soap and water are not available

Warnings

For External Use only

Flammable. Keep away from heat or flame

Do not Use

On children less than 2 months of age- On open skin wounds -around eyes -in ears and mouth

When using this product

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. -avoid contact with broken skin. - do not inhale or ingest

Stop use and ask a doctor if

Irritation or rash occurs

­­­­­ Keep out of reach of children

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

Directions

-Place enough product on hands to cover all surfaces. Rub hands together until dry. -Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

Store between 15-30C (59-86F). -Avoid freezing and excessive above 40C (104F)

Inactive Ingredients

Aloe Barbadensis (leaf) Extract, Carbomer, Fragrance, Glycerin, purified water

Eddie’s Clean Hand Sanitizer

Gel

EDDDIES HAND SANITIZER GEL 
alcohol 75% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73761-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL177.75 mL  in 237 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73761-102-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product03/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/02/2020
Labeler - Nutralife Biosciences, Inc (078834338)
Registrant - Nutralife Biosciences, Inc (078834338)

Revised: 3/2020
Document Id: a1c2f26f-3689-1751-e053-2a95a90ae63f
Set id: a1c2f26f-3688-1751-e053-2a95a90ae63f
Version: 1
Effective Time: 20200326
 
Nutralife Biosciences, Inc