Advanced Hand Sanitizer: Package Insert and Label Information

ADVANCED HAND SANITIZER- alcohol liquid
Flex Beauty Labs, LLC

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.

Ethyl Alcohol 62.0%

Purpose

Antimicrobial

Uses

Hand Santizer to help reduce bacteria on skin that may cause disease.

Warnings

Flammable. Keep away from heat or flame.

For external use only.

Keep out of reach of children.

When using this product,

do not use in or near the eyes. In case of contact, rinse eyes thoroughtly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach for children.

If swallowed, get medical help or contact a Posion Control Center right away.

Directions:

. Place enough Product in your palm to thoroughtly spread on both hands and rub into the skin until dry.

. Children under 6 years of age should be supervised when using this product.

Other Information:

. Store below 106℉. (41℃)

Inactive Ingredients:

Water (Aqua), Aloe Vera Leaf , Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine,

advance hand sanitizer
(click image for full-size original)

ADVANCED HAND SANITIZER
hand sanitizer liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:72308-001
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (ALCOHOL) ALCOHOL 62 mL in 1 mL
Inactive Ingredients
Ingredient Name Strength
ALOE VERA LEAF
CARBOXYPOLYMETHYLENE
GLYCERIN
PROPYLENE GLYCOL
.ALPHA.-TOCOPHEROL ACETATE
TROLAMINE
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:72308-001-01 295 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 08/02/2017
Labeler — Flex Beauty Labs, LLC (080858917)

Revised: 05/2018 Flex Beauty Labs, LLC

DrugInserts.com provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by DrugInserts.com. Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

As the leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. Our material is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2021. All Rights Reserved.