ALCOHOL PREP PADS- isopropyl alcohol swab

Alcohol Prep Pads by

Drug Labeling and Warnings

Alcohol Prep Pads by is a Otc medication manufactured, distributed, or labeled by Cardinal Health 200, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Isopropyl Alcohol USP, 70% v/v

Purpose

Antiseptic

Uses

For preparation of skin prior to injection

Warnings

For external use only

Flammable. Keep away from fire or flame

Do not use

• with electrocautery procedures
• in the eyes
• on mucus membrane
• on irritated skin
  

Stop use and ask doctor if

• irritation or redness develops
• if condition persists for more than 72 hours
  

Caution

In case of deep or punctured wounds, consult a doctor

Keep out of reach of children

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

Directions for use

• wipe injection site vigorously and discard
  

Inactive Ingredient

purified water

Principal Display Panel

CardinalHealth

NDC: 63517-600-01

REF MW-APM100

alcohol prep pads

EN - Medium 70% Isopropyl alcohol prep pad

FR - Tampon imbibe d'alcool isopropylique a 70%, moyen

ES - Almohadilla mediana impregnada en alcohol isopropilico al 70%

CardinalHealth

X100

CardinalHealth

NDC: 63517-600-02

REF MW-APM

alcohol prep pads

EN - Medium 70% Isopropyl alcohol prep pad

FR - Tampon imbibe d'alcool isopropylique a 70%, moyen

ES - Almohadilla mediana impregnada en alcohol isopropilico al 70%

CardinalHealth

X200

CardinalHealth

NDC: 63517-600-50

REF MW-APM50

alcohol prep pads

EN - Medium 70% Isopropyl alcohol prep pad

FR - Tampon imbibe d'alcool isopropylique a 70%, moyen

ES - Almohadilla mediana impregnada en alcohol isopropilico al 70%

CardinalHealth

X50

INGREDIENTS AND APPEARANCE

ALCOHOL PREP PADS  
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63517-600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63517-600-50	50 in 1 CARTON	02/08/2016
1		1 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 63517-600-01	100 in 1 CARTON	02/08/2016
2		1 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 63517-600-02	200 in 1 CARTON	02/08/2016
3		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	02/08/2016

Labeler - Cardinal Health 200, Inc. (961027315)

Registrant - Cardinal Health 200, Inc. (961027315)