DERMACEN LOTIONIZED HAND SANITIZER- alcohol liquid

DermaCen Lotionized Hand Sanitizer by

Drug Labeling and Warnings

DermaCen Lotionized Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Central Solutions Inc, Central Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol 70%

Purpose

Antiseptic

Uses

• An effective antimicrobial hand cleanser for topical application
• Recommended for repeated use
• Reduces transient microorganisms on intact skin
• Keeps hands from drying out due to repeated uses

Warnings

• For External Use Only.
• Flammable, keep away from fire or open flame

When using this product:

• Avoid contact with eyes
• In case of eye contact, flush with water for 15 nibutes
• Discontinue use and see a doctor if irritation occurs
• Avoid contact with broken skin

Keep out of reach of children.

Directions

• Wet hands thoroughly with product. Allow to dry without wiping. Use no water or towels

Other information

• Not tested on animals

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Butylene Glycol, Calcium Pantothenate (Vitamin B5), Cetyl Alcohol, Fragrance, Glycerin, Glyceryl Laurate, Hydroxypropyl Cellulose, Isopropyl Myristate, Maltodextrin, Niacinamide (Vitamin B3), Pyridoxine HCl (Vitamin B6), Silica, Sodium Ascorbyl Phosphate (Vitamin C),Sodium Starch Octenylsuccinate, Titanium Dioxide, Tocopherol (Vitamin E), Tocopheryl Acetate (Vitamin E), Trehalose, Water

Questions?

Call 800-255-0262

PRINCIPAL DISPLAY PANEL

NDC: 62654-151-64

DermaCen

Lotionized

Hand

Sanitizer

For hand washing

to decrease bacteria

on the skin

Net Contents:

8 oz (236mL)

INGREDIENTS AND APPEARANCE

DERMACEN LOTIONIZED HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62654-151
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
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TOCOPHEROL (UNII: R0ZB2556P8)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETYL ALCOHOL (UNII: 936JST6JCN)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
OCTENYLSUCCINIC ACID (UNII: 12UZE4X73L)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
TREHALOSE (UNII: B8WCK70T7I)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL LAURATE (UNII: Y98611C087)
NIACINAMIDE (UNII: 25X51I8RD4)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62654-151-64	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/07/2024

Labeler - Central Solutions Inc (007118524)

Registrant - Central Solutions (007118524)

Establishment
Name	Address	ID/FEI	Business Operations
Central Solutions Inc		007118524	manufacture(62654-151)