MUSE HEALTH HAND SANITIZER - FRAGRANCE FREE- ethyl alcohol gel

Muse Health Hand Sanitizer - Fragrance Free by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 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 if

Irritation and redness develop

Condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

If swallowed, get meidcal 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, Ammonium polyacryloyldimethyl taurate, Citrus Aurantifoila Oil

Questions?

feedback@musehealth.com

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INGREDIENTS AND APPEARANCE

MUSE HEALTH HAND SANITIZER - FRAGRANCE FREE 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71683-012
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)
WATER (UNII: 059QF0KO0R)
LIME OIL (UNII: UZH29XGA8G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71683-012-01	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	part333E	08/06/2020

Labeler - CC Wellness, LLC (067692292)

Establishment
Name	Address	ID/FEI	Business Operations
CC Wellness, LLC		067692292	manufacture(71683-012)