HAND SANITIZER- lotionized hand sanitizer lotion

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by McKesson Medical-Surgical, Central Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active Ingredient
Ethanol 70%

PURPOSE

Purpose
Antiseptic

INDICATIONS & USAGE

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

Warnings

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

STOP USE

When using this product:

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

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

towels

OTHER SAFETY INFORMATION

Other information

• Not tested on animals

INACTIVE INGREDIENT

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

Questions?
Call 1-800-777-4908

PRINCIPAL DISPLAY PANEL

68599-5207-1

Thera Lotionized Hand Sanitizer

An antiseptic hand sanitizer with moisturizers and
emollients to help prevent drying of the skin.

NET CONTENTS 8 fl oz (237 mL)

MFR # 53-LHS8

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
lotionized hand sanitizer lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68599-5207
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
GLYCERYL LAURATE (UNII: Y98611C087)
OCTENYLSUCCINIC ACID (UNII: 12UZE4X73L)
WATER (UNII: 059QF0KO0R)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TOCOPHEROL (UNII: R0ZB2556P8)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TREHALOSE (UNII: B8WCK70T7I)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
CETYL ALCOHOL (UNII: 936JST6JCN)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CALCIUM PANTOTHENATE (UNII: 568ET80C3D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68599-5207-1	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/17/2024

Labeler - McKesson Medical-Surgical (023904428)

Establishment
Name	Address	ID/FEI	Business Operations
Central Solutions		007118524	manufacture(68599-5207)