MCKESSON ANTISEPTIC HAND SANITIZER- ethyl alcohol gel

McKesson Antiseptic Hand Sanitizer by

Drug Labeling and Warnings

McKesson Antiseptic Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by McKesson Medical-Surgical, Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient (in each gram)

Ethyl Alcohol 66.5%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

• for handwashing to reduce bacteria on skin whenever soap and water are not available
• reduces bacteria that potentially can cause disease or infection
• recommended for repeated use

WARNINGS

Warnings

Flammable. keep away from fire of flame.

For external use only

DO NOT USE

Do not use

• in the eyes. In case of contact, rinse thoroughly with water.

STOP USE

Stop use and ask a doctor if

• irritation and redness develops and persist for 72 hours

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.

DOSAGE & ADMINISTRATION

Directions

• wet hands thoroughly with product and allow to dry without wiping
• children under 6 years of age should be supervised while using this product

OTHER SAFETY INFORMATION

Other information

• store at 59-86ºF (15-30ºC)
• tamper evident. Do not use if packet is torn, cut or opened.

INACTIVE INGREDIENT

Inactive ingredients

aloe vera, carbomer, DD&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

QUESTIONS

Questions or comments? Call 1-800-777-4908

PRINCIPAL DISPLAY PANEL

NDC: 68599-1120-1

McKesson

Antiseptic Hand Sanitizer

Individual Packets

Ethyl Alcohol 66.5% | With Aloe

Instant hand sanitizer with soothing aloe and a fresh scent.

NET WT 0.9 g

144 Packs Per Box

Do Not Reuse

MFR # 82482

INGREDIENTS AND APPEARANCE

MCKESSON ANTISEPTIC HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68599-1120
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	665 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
TROLAMINE (UNII: 9O3K93S3TK)
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68599-1120-1	144 in 1 BOX	10/04/2021
1		0.0009 L in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/04/2021

Labeler - McKesson Medical-Surgical (023904428)

Registrant - Unifirst First Aid Corporation (832947092)