ALLOUT NANO- isopropyl alcohol gel 
SERENITY TECHNOLOGIES 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.

----------

ALLOUT™ NANO

DRUG FACTS

ACTIVE INGREDIENTS

ISOPROPYL ALCOHOL 75% v/v.

PURPOSE

ANTISEPTIC

USES

HAND SANITIZER TO HELP REDUCE GERMS ON THE SKIN WHEN SOAP AND WATER ARE NOT AVAILABLE.

WARNINGS

FLAMMABLE, KEEP AWAY FROM FIRE AND FLAMES. FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT KEEP OUT OF EYES. IN CASE OF CONTACT WITH EYES RINSE EYES THOROUGHLY WITH WATER.

STOP USE AND ASK A DOCTOR IF IRRITATION AND REDNESS DEVELOP AND CONDITION PERSISTS FOR 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 PRODUCT TO HANDS THOROUGHLY, RUB HANDS TOGETHER UNTIL DRY.

OTHER INFO

INACTIVE INGREDIENTS

ALOE BARBADENSIS LEAF EXTRACT, ALUM, COPPER, ESTER, GLYCERINE, HYALURONIC ACID, HYDROXYPROPYL CELLULOSE, SILVER, WATER, WHITE CAMPHOR OIL, ZINC.

QUESTIONS?

+1 (951)-587-3753

WWW.ALLOUTNANO.COM

Manufactured By:
Serenity Technologies Inc.
43320 Business Park Dr., B105
Temecula, CA 92590

PRINCIPAL DISPLAY PANEL - 59.1 ml Bottle Label

NANOTECHNOLOGY

ALLOUT™
NANO

ADVANCED
HAND SANITIZER

LONG LASTING
ANTIMICROBIAL PROTECTION
FORMULATED WITH
COPPER, SILVER AND ZINC

GEL

SKIN NOURISHING
WITH HYALURONIC ACID

CLEAN HANDS
COUNT

2 fl oz (59.1 ml)

PRINCIPAL DISPLAY PANEL - 59.1 ml Bottle Label
ALLOUT NANO 
isopropyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75814-104
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL75 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POTASSIUM ALUM (UNII: 1L24V9R23S)  
SILVER (UNII: 3M4G523W1G)  
COPPER (UNII: 789U1901C5)  
PYRITHIONE ZINC (UNII: R953O2RHZ5)  
CAMPHOR OIL, WHITE (UNII: 26P3H26Z9X)  
HYALURONIC ACID (UNII: S270N0TRQY)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
LAURYL LACTATE (UNII: G5SU0BFK7O)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75814-104-0129.6 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/04/2020
2NDC:75814-104-0259.1 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/04/2020
3NDC:75814-104-06177.4 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/04/2020
4NDC:75814-104-08236.6 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/04/2020
5NDC:75814-104-341000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/04/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/04/2020
Labeler - SERENITY TECHNOLOGIES INC. (829399240)

Revised: 8/2020
Document Id: 0d30a5c7-c011-491f-9950-f99d6058a269
Set id: 0c75f995-4082-4d73-af2c-ca1522c2c8d9
Version: 1
Effective Time: 20200810
 
SERENITY TECHNOLOGIES INC.