OTC Medication Information: Aevi Here and Now Hand Sanitizer

AEVI HERE AND NOW HAND SANITIZER- 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.

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
(click image for full-size original)
AEVI HERE AND NOW HAND SANITIZER
ethyl alcohol spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4202
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 70 mL in 100 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
EUCALYPTUS OIL
PINE NEEDLE OIL (PINUS SYLVESTRIS)
ROSMARINUS OFFICINALIS FLOWERING TOP OIL
LIMONENE, (+)-
WATER
ALOE VERA LEAF
LINALOOL, (+/-)-
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:62742-4202-1 237 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 02/18/2021
Labeler — Allure Labs Inc (926831603)
Registrant — Allure Labs Inc (926831603)
Establishment
Name Address ID/FEI Operations
Allure Labs Inc 926831603 manufacture (62742-4202)

Revised: 03/2021 Allure Labs Inc

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2022. All Rights Reserved.