MEDI-FIRST PLUS STERILE ALCOHOL PADS- isopropyl alcohol liquid

MEDI-FIRST PLUS STERILE ALCOHOL PADS by

Drug Labeling and Warnings

MEDI-FIRST PLUS 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 use to decrease germs 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 or 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

• protect from freezing and avoid excessive heat
  

Inactive ingredient

water

Questions?

Call 1-800-634-7680

Medi-First Plus Alcohol Wipes Label

Medi-First Plus® Alcohol Wipes

Sterile

50 Wipes

INGREDIENTS AND APPEARANCE

MEDI-FIRST PLUS STERILE ALCOHOL PADS 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-931
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: 47682-931-50	50 in 1 BOX	12/23/2011
1		0.8 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 47682-931-51	4000 in 1 CASE	12/23/2011	08/16/2017
2		0.8 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	12/23/2011

Labeler - Unifirst First Aid Corporation (832947092)

Establishment
Name	Address	ID/FEI	Business Operations
Phoenix Innovative Healthcare Manufacturers		650687176	manufacture(47682-931) , relabel(47682-931) , repack(47682-931)