ALCOHOL WIPE- isopropyl alcohol swab ALCOHOL PREP PAD- isopropyl alcohol swab

Alcohol Prep Pad by

Drug Labeling and Warnings

Alcohol Prep Pad by is a Otc medication manufactured, distributed, or labeled by Honeywell Safety Products USA, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Isopropyl alcohol 70%

Purpose

First aid antiseptic

Uses

first aid to help prevent infection in minor cuts, scrapes, and burns

Warnings

For external use only

Flammable, keep away from fire and flame

Do not use

• in or near eyes
• over large areas of the body

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

When using this product

• do not use longer than 1 week unless directed by a doctor

Stop use and consult a doctor if

• condition persists or gets worse

Keep out of the reach of children

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

Directions

• clean the affected area
• may be covered with a sterile bandage
• apply wipe to affeted are 1 to 3 times daily
• discard wipe after single use

Other information

• store at room temperature 15 o to 25 o C (59 o to 77 oF)
• do not use if packet is torn or opened

Inactive ingredient

water

Questions

1-800-430-5490

alcohol wipes

Alcohol wipes 10 ct

OH Pak

INGREDIENTS AND APPEARANCE

ALCOHOL WIPE 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-0143
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: 0498-0143-04	0.4 mL in 1 POUCH; Type 0: Not a Combination Product	09/18/2018
2	NDC: 0498-0143-34	10 in 1 BOX	09/18/2018
2		0.4 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 0498-0143-05	50 in 1 BOX	09/18/2018
3		0.4 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 0498-0143-10	100 in 1 BOX	09/18/2018
4		0.4 mL in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 0498-0143-33	3000 in 1 BOX	09/18/2018
5		0.4 mL in 1 POUCH; 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	09/18/2018

ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0498-0142
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: 0498-0142-34	10 in 1 BOX	01/01/2017
1		0.4 mL in 1 POUCH; 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	01/01/2017

Labeler - Honeywell Safety Products USA, Inc (079287321)

Registrant - Honeywell Safety Products USA, Inc (079287321)

Establishment
Name	Address	ID/FEI	Business Operations
Honeywell Safety Products USA, Inc		079287321	pack(0498-0142, 0498-0143)