MUSE HEALTH HAND SANITIZER- ethyl alcohol gel

Muse Health Hand Sanitizer by

Drug Labeling and Warnings

Muse Health Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by CC Wellness, CC Wellness, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alocohol 62% by wt.

PURPOSE

Antiseptic

Uses

To decrease bacteria on the skin that could cause disease.

Recommended for repeated use.

WARNINGS

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

Keep out of eyes.

In case of contact with eyes, flush thoroughly with water.

Avoid contact with broken skin.

Do not inhale or ingest.

Stop use and ask a doctor

Irritation and redness develop

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

Wet hands thoroughly with product and allow to dry without wiping.

For children under 6, use only under adult supervision.

Not recommended for infants.

Other Information

Do not store above 105°

May discolor some fabrics

Harmful to wood finishes and plastics

INACTIVE INGREDIENT

Water (Aqua), Glycerin, Tocopheryl Acetate, Isopropyl Palmitate, Acrylates Copolymer, Aminomethyl Propranolol, Parfum

Questions?

feedback@musehealth.com

Principle Display Panel

INGREDIENTS AND APPEARANCE

MUSE HEALTH HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71683-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71683-011-01	240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/06/2020

Labeler - CC Wellness (067692292)

Establishment
Name	Address	ID/FEI	Business Operations
CC Wellness, LLC		067692292	manufacture(71683-011)