MCKESSON ALCOHOL PREP PAD- isopropyl alcohol swab

McKesson Alcohol Prep Pad by

Drug Labeling and Warnings

McKesson Alcohol Prep Pad by is a Otc medication manufactured, distributed, or labeled by McKesson Medical-Surgical, Shandong Haiyan Medical, Jiangsu Province Jianerkang Medical Dressing Co., Ltd, Phoenix Innovative Healthcare, Lights Medical Manufacture Co. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Isopropyl Alcohol 70% v/v

Purpose

First Aid Antiseptic

Use

For preparation of the skin prior to an injection

Warnings

• For external use only
• Flammable, keep away from fire or flame

DO NOT USE

• Do not use with electrocautery procedures
• Do not use in the eyes
• Do not apply to irritated skin

• Stop use if pain, irritation, redness, or swelling occurs, discontinue use and consult a physician.

• Keep out from reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Open packet
• Remove pad
• Apply topically as needed to cleanse intended area. Discard after single use.

Other information

• Store at room temperature 59-86°F (15-30°C)
• Contents sterile in unopened, undamaged package

Inactive ingredients

purified water

Principal Display Panel – Box Label

NDC: 68599-5804-2

MCKESSON

Alcohol Prep Pads

STERILE | SATURATED WITH 70% v/v ISOPROPYL ALCOHOL

1.2" x 2.6"
(3 cm x 6.5 cm)

200
PER BOX

DO NOT REUSE

MFR# 58-204

Principal Display Panel – Packet Label

NDC: 68599-5804-1

MCKESSON

Alcohol Prep Pad

STERILE | SATURATED WITH
70% v/v ISOPROPYL ALCOHOL

1.2" x 2.6"
(3 cm x 6.5 cm)

DO NOT
REUSE

MFR# 58-204

INGREDIENTS AND APPEARANCE

MCKESSON ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68599-5804
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68599-5804-3	20 in 1 CASE	04/09/2010
1	NDC: 68599-5804-2	200 in 1 BOX
1	NDC: 68599-5804-1	1 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 68599-5804-6	10 in 1 CASE	04/09/2010
2	NDC: 68599-5804-5	100 in 1 BOX
2	NDC: 68599-5804-4	1 mL 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 not final	part333A	04/09/2010

Labeler - McKesson Medical-Surgical (023904428)