PREMIUM HAND SANITIZER WITH ALOE- ethanol gel

Premium Hand Sanitizer with Aloe by

Drug Labeling and Warnings

Premium Hand Sanitizer with Aloe by is a Otc medication manufactured, distributed, or labeled by MCKESSON MEDICAL-SURGICAL INC., Central Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                         Purpose

Ethanol 70% ......................... hand sanitizer

PURPOSE

Uses

• an antiseptic hand sanitizer for topical application
• helps prevent infection and cross-contamination
• reduces transient microorganisms on intact skin
• recommended for repeated use

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.

INDICATIONS & USAGE

McKesson Premium Hand Sanitizer with Aloe

With Vitamin E, Moisturizers, & Emollients

for frequent use

DOSAGE & ADMINISTRATION

Directions

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

WARNINGS

Warnings

For external use only.

Flammable, keep away from fire or flame.

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.

INACTIVE INGREDIENT

Inactive Ingredients

purified water, carbomer, isopropanol, glycerin, aloe barbadensis leaf juice, tocopherol (vitamin E), isopropyl myristate, diisopropyl sebacate, propylene glycol, aminomethyl propanol, fragrance, yellow 5, blue 1.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PREMIUM HAND SANITIZER WITH ALOE 
ethanol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68599-5202
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68599-5202-1	59 g in 1 PACKAGE; Type 0: Not a Combination Product	01/09/2015
2	NDC: 68599-5202-2	118 g in 1 PACKAGE; Type 0: Not a Combination Product	01/09/2015
3	NDC: 68599-5202-3	237 g in 1 PACKAGE; Type 0: Not a Combination Product	01/09/2015
4	NDC: 68599-5202-4	532 g in 1 PACKAGE; Type 0: Not a Combination Product	01/09/2015
5	NDC: 68599-5202-5	1000 g in 1 PACKAGE; Type 0: Not a Combination Product	01/09/2015
6	NDC: 68599-5202-6	237 g in 1 BOTTLE; Type 0: Not a Combination Product	01/09/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/09/2015

Labeler - MCKESSON MEDICAL-SURGICAL INC. (023904428)