ALCOHOL PAD- isopropyl alcohol swab

Alcohol Pad by

Drug Labeling and Warnings

Alcohol Pad by is a Otc medication manufactured, distributed, or labeled by McKesson. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Isopropyl Alcohol 70% v/v

PURPOSE

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

• with electrocautery procedures
• in the eyes

Stop use

if irritation and redness develop

Ask a doctor

if condition persists for more than 72 hours

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

Wipe injection site vigorously and discard

SPL UNCLASSIFIED SECTION

OTHER INFORMATION

Store at room temperature 15° - 30° C (59° - 86° F)

INACTIVE INGREDIENT

purified water

QUESTIONS

PACKAGE INFORMATION

Sunmark®

COMPARE TO B-D® ACTIVE INGREDIENTS*

NDC: 49348-077-53

Alcohol Prep Pads

Antiseptic for preparation of the skin prior to injection

Isopropyl alcohol, 70%

100 INDIVIDUALLY WRAPPED FOIL PACKETS
1.25 X 1.25 IN (2.9 X 3.2 cm)

Distributed by McKesson
One Post Street
San Francisco, CA 94104
Money Back Guarantee

*This product is not namufactured or distributed by Beckton Dickson, owner of the registered trademark, B-D®.

INGREDIENTS AND APPEARANCE

ALCOHOL PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49348-077
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Isopropyl alcohol (UNII: ND2M416302) (Isopropyl alcohol - UNII:ND2M416302)	Isopropyl alcohol	0.70 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49348-077-53	100 in 1 BOX
1		1 in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/19/2003

Labeler - McKesson (177667227)