SANIX ALCOHOL HAND RUB- alcohol liquid

Sanix Alcohol Hand Rub by

Drug Labeling and Warnings

Sanix Alcohol Hand Rub by is a Otc medication manufactured, distributed, or labeled by Topiderm, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

Ethyl Alcohol 62% (v/v)

Purpose

Antimicrobial

Uses

Hand sanitizer for reduction of bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from fire and flame.

Keep out of and away from the eyes. In case of eye contact flush thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. Not for use on infants.

If product is swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Apply enough product into the palm and rub hands together to thoroughly wet them

• Continue until the product dries without wiping off
• Supervise children when they are using the product
• Store below 110°F (43°C)
• May discolor some types of fabrics & surfaces.

Inactive ingredients

Water, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate, Polysorbate 20, Isopropyl Alcohol, Isopropyl Palmitate, Tetrahydroxypropyl Ethylenediamine, Carbomer, Fragrance.

PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label

ANTIBACTERIAL
Hand Sanitizer Gel
by REPLENIX®

Kills 99.9% of Most Illness Causing Germs*
Triple Action Moisturizers
Softens Hands with Aloe, Vitamin E & Glycerin

Made in USA
Trusted By
MEDICAL
PROFESSIONALS
Manufactured by Topix Pharmaceuticals

Net 8 fl.oz. (237ml)

INGREDIENTS AND APPEARANCE

SANIX ALCOHOL HAND RUB 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51326-900
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	0.62 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Isopropyl palmitate (UNII: 8CRQ2TH63M)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
WATER (UNII: 059QF0KO0R)
EDETOL (UNII: Q4R969U9FR)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
Polysorbate 20 (UNII: 7T1F30V5YH)
Glycerin (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51326-900-08	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333E	03/17/2020

Labeler - Topiderm, Inc. (049121643)