ELYPTOL LIGHT SCENT- ANTIMICROBIAL HAND GEL- ethanol gel 
ELYPTOL 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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Elyptol Light Scent- Antimicrobial Hand Gel

Drug Facts

Active ingredient:

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Keep out reach of children

If swallowed, seek medical advice or contact a Poison Control Center immediately.

Uses

Warnings

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

When using this product
keep away from eyes. In case of eye contact, rinse eyes with water.

Stop use and ask a doctor if
redness or irritation develops. If issues persist, seek medical attention.

Directions

Other information

Inactive ingredients

Aqua (Purified Water), Eucalyptol, Glycerin, Hydroxypropylcellulose, Piroctone Olamine.

Questions?(888) 424-9874

Moisturizing Hand Sanitizer

NATURAL INGREDIENTS

SUITABLE FOR HIGH FREQUENCY USE

KILLS 99.99% of GERMS

NO NEED TO RINSE

Dermatologically Tested

Not Tested On Animals

Packaging

15ml (0.5 fl oz)2ml (0.06 fl oz)144 count - 2ml (0.06 fl oz)image description

ELYPTOL LIGHT SCENT- ANTIMICROBIAL HAND GEL 
ethanol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69343-421
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL7 mL  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
EUCALYPTOL (UNII: RV6J6604TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYPROPYL CELLULOSE (1600000 WAMW) (UNII: RFW2ET671P)  
PIROCTONE OLAMINE (UNII: A4V5C6R9FB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69343-421-021 in 1 CARTON06/01/2016
159 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:69343-421-081 in 1 CARTON06/01/2016
2236 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:69343-421-161 in 1 CARTON06/01/2016
3473 mL in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:69343-421-321 in 1 CARTON06/01/2016
4946 mL in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:69343-421-011 in 1 CARTON01/13/2017
52 mL in 1 PACKET; Type 0: Not a Combination Product
6NDC:69343-421-151 in 1 CARTON01/13/2017
615 mL in 1 BOTTLE; Type 0: Not a Combination Product
7NDC:69343-421-421 in 1 CARTON06/01/2016
71242 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/2016
Labeler - ELYPTOL INC. (079594781)

Revised: 12/2022
Document Id: d8b2683b-636f-482f-8943-736c5a441097
Set id: 3d148ce6-e6ac-4baa-937a-cce49de182a5
Version: 9
Effective Time: 20221219
 
ELYPTOL INC.