GREEN GUARD STERILE ALCOHOL PADS- isopropyl alcohol liquid

Green Guard Sterile Alcohol Pads by

Drug Labeling and Warnings

Green Guard Sterile Alcohol Pads by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation, Phoenix Innovative Healthcare Manufacturers. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl alcohol 70% v/v

Purpose

Antiseptic

Uses

• for preparation of the skin prior to injection
• first aid to help prevent infection in minor cuts, scrapes and burns
  

Warnings

Flammable, keep away from fire or flame.

For external use only.

Do not use

• with electrocautery procedures
• in or near the eyes
• longer than 1 week unless directed by a doctor

In case of deep puncture wounds, animal bites or serious burns, consult a doctor.

Stop use and ask a doctor if

• irritation and redness develops
• 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 or
• apply to cut, scrape or burn and discard after single use
  

Other information

• store at room temperature 59° F to 86° F (15° C to 30° C )

Inactive ingredient

water

Questions?

Call 1-800-869-6970

Green Guard Alcohol Wipes Label

Sterile Alcohol Wipes

First aid to help ptrevent

infection in minor cuts,

scrapes and burns

Green Guard®

Order # 3015

50 wipes per box

INGREDIENTS AND APPEARANCE

GREEN GUARD STERILE ALCOHOL PADS 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-019
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: 47682-019-50	50 in 1 BOX	04/25/2012
1		0.45 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 47682-019-51	200 in 1 BOX	04/25/2012	08/07/2017
2		0.45 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 47682-019-52	4000 in 1 CASE	04/25/2012	08/07/2017
3		0.45 mL in 1 PACKAGE; 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	12/23/2011

Labeler - Unifirst First Aid Corporation (832947092)

Establishment
Name	Address	ID/FEI	Business Operations
Phoenix Innovative Healthcare Manufacturers		650687176	manufacture(47682-019) , relabel(47682-019) , repack(47682-019)