805 Medline Sterile Isopropyl Prep Pads

Medline Alcohol Prep by

Drug Labeling and Warnings

Medline Alcohol Prep by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MEDLINE ALCOHOL PREP STERILE, MEDIUM- isopropyl alcohol swab 
Medline Industries, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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805 Medline Sterile Isopropyl Prep Pads

Active ingredient

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic

Uses

• for preparation of the 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

Stop use and ask a doctor if

• Irritation and redness develops
• Condition gets worse or 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.

Other information

Protect from freezing and avoid excessive heat.

Inactive ingredients

Water

Package/Label Principal Display Panel

MEDLINE PREP PADS

STERILE

REF MDS090735

MEDIUM PREP PADS

Alcohol Antiseptic

This product is not made with natural rubber latex

• Saturated with 70% Isopropyl Alcohol

  Medium

  2-Ply Pad

  Individually wrapped

Qty 200

Package/Label Back

MEDLINE ALCOHOL PREP  STERILE, MEDIUM
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-805
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: 53329-805-60	200 in 1 BOX	01/01/2007	12/31/2019
1		1 in 1 PACKET
1		5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 53329-805-97	3000 in 1 CASE	01/01/2007	12/31/2017
2		1 in 1 PACKET
2		5 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 53329-805-09	1 in 1 PACKET	01/01/2007	12/31/2019
3		5 mL in 1 APPLICATOR; 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	01/01/2007	12/31/2019

Labeler - Medline Industries, Inc. (025460908)

Revised: 1/2020

Document Id: 9d5d6026-f1dc-eafd-e053-2995a90afcf1

34390-5

Set id: 9a8584e1-b422-4b77-8464-4e022d578fad

Version: 10

Effective Time: 20200130