AEVI HERE AND NOW HAND SANITIZER- ethyl alcohol spray 
Allure Labs 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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Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antimicrobial

Uses:

Helps to reduce bacteria on the skin. For repeat use.

Warnings

For external use only. Flammable, keep away from heat and flame. Do not store above 104ºF/40ºC.

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

• Avoid contact with broken skin.

Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center immediately.

Directions:

Apply all over your hands and allow to dry. Do not rinse off. For children under 6, use only under adult supervision. Not recommended for infants.

Inactive Ingredients

Aqua (Water), Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Pinus Sylvestris Leaf (Nordic Pine) Oil, Eucalyptus Globulus Leaf Oil*, Rosmarinus Officinalis (Rosemary) Oil, Linalool, Limonene.

Aevi Wellness, Inc
251 Little Falls Drive
Wilmington, DE 19808
Made in USA

IMGAVHS

AEVI HERE AND NOW HAND SANITIZER 
ethyl alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4202
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)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)  
ROSMARINUS OFFICINALIS FLOWERING TOP OIL (UNII: OXN0D3N28L)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62742-4202-1237 mL in 1 BOTTLE; Type 0: Not a Combination Product02/18/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/18/2021
Labeler - Allure Labs Inc (926831603)
Registrant - Allure Labs Inc (926831603)
Establishment
NameAddressID/FEIBusiness Operations
Allure Labs Inc926831603manufacture(62742-4202)

Revised: 3/2021
Document Id: bc82d262-137a-a7cb-e053-2995a90a700a
Set id: bc83008b-2602-1c09-e053-2a95a90a45c3
Version: 1
Effective Time: 20210301
 
Allure Labs Inc