HAND SANITIZER ADVANCE- alcohol gel

Hand Sanitizer Advance by

Drug Labeling and Warnings

Hand Sanitizer Advance by is a Otc medication manufactured, distributed, or labeled by Comercializadora Mca, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 70% v/v.

Purpose

Antiseptic

Use

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Water, carboner, triethanolamine, glycerine, propylene glycol, fragrance, aloe barbadensis leaf juice.

Made in Mexico by COMERCIALIZADORA MCA SA DE CV, LEON, GTO, MEXICO.
Questions? salesmx@besser-chem.com

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER ADVANCE 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80717-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
BACKHOUSIA CITRIODORA LEAF OIL (UNII: 2UQQ0PI06P)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80717-001-01	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/08/2020

Labeler - Comercializadora Mca, S.A. de C.V. (814408050)