FOAMING INSTANT HAND SANITIZER WITH ALOE- ethanol gel

Foaming Instant Hand Sanitizer with Aloe by

Drug Labeling and Warnings

Foaming Instant Hand Sanitizer with Aloe by is a Otc medication manufactured, distributed, or labeled by MCKESSON MEDICAL-SURGICAL INC., Central Solutions Inc. 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 Foaming Hand Sanitizer with Aloe

With Moisturizers & Emollients

With Pump

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, DEA-C8-18 perfluoroalkylethyl phosphate, glycereth-26, aloe barbadensis leaf juice, fragrance, citric acid.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FOAMING INSTANT HAND SANITIZER WITH ALOE 
ethanol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68599-5205
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)
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)
GLYCERETH-26 (UNII: NNE56F2N14)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68599-5205-1	251 g in 1 PACKAGE; Type 0: Not a Combination Product	10/24/2017
2	NDC: 68599-5205-2	1000 g in 1 PACKAGE; Type 0: Not a Combination Product	10/24/2017

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)

Establishment
Name	Address	ID/FEI	Business Operations
Central Solutions Inc		007118524	manufacture(68599-5205)