Ellipse™ Hand Sanitizer Caribbean Scent

Ellipse Hand Sanitizer by

Drug Labeling and Warnings

Ellipse Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Genomma Lab USA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ELLIPSE HAND SANITIZER  CARIBBEAN SCENT- alcohol liquid 
Genomma Lab USA

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Ellipse™ Hand Sanitizer
Caribbean Scent

Drug Facts

Active Ingredient

Ethyl Alcohol 70 % v/v

Purpose

Antiseptic

Uses

  • To decrease Bacteria on the skin when water, soap & towel are not available
  • Recommended for repeated use.

Warnings

  • For external use only
  • Flammable. Keep away from fire or flame.

When using this product

  • Keep out of eyes. In case of contact with eyes, rinse eyes thoroughly with water
  • Do not use on broken or irritated skin.

Stop use and ask a doctor if irritation or redness develop and last more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply enough product to wet hands. Rub hands together until dry. Supervise children in use of this product.

Other information

  • Do not store above 105 °F (40 °C)
  • May discolor certain fabrics and wood surfaces.

Inactive Ingredients

Water, Glycerin, Fragrance, Organic Aloe Barbadensis Leaf Juice, FD&C Blue 1.

Questions?

Call Toll Free: 1-877-994-3666

Distributed by Genomma Lab USA, Inc. Houston, TX, 77027.

PRINCIPAL DISPLAY PANEL - 38 mL Bottle Carton

ellipse™
Hand Sanitizer

Caribbean Sea Scent

1.28 fl oz
(38 mL)

PRINCIPAL DISPLAY PANEL - 38 mL Bottle Carton
ELLIPSE HAND SANITIZER   CARIBBEAN SCENT
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 50066-611
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
alcohol (UNII: 3K9958V90M) (alcohol - UNII:3K9958V90M) alcohol70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Glycerin (UNII: PDC6A3C0OX)  
Water (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Product Characteristics
ColorBLUE (light blue) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 50066-611-021 in 1 CARTON07/22/202101/28/2025
138 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph drugM00307/22/202101/28/2025
Labeler - Genomma Lab USA (832323534)

Revised: 1/2025
 

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