MEDI-FIRST ALCOHOL WIPES- isopropyl alcohol, 70% swab

Medi-First Alcohol Wipes by

Drug Labeling and Warnings

Medi-First Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient
Isopropyl Alcohol, 70%

PURPOSE

Purpose

Anticeptic

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

• for external use only
• flammable, keep away from fire or flame

Do not use

• with electrocautery procedures
• in the eyes. If contact occurs, flush eyes with water.

Stop use and ask a doctor if

• irritation and redness develops
• condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

Directions

• wipe injection site vigorously and discard
• apply to cut, scrape or burn and discard after single use

OTHER SAFETY INFORMATION

Other information

• store at room temperature 59º-86ºF (15º-30ºC)
• tamper evident sealed packets
• do not use any open or torn packets

INACTIVE INGREDIENT

Inactive ingredients

purified water

QUESTIONS

Questions or comments?
1-800-634-7680

Medi-First Alcohol Wipes Label

Medi-First®

Alcohol Wipes

Sterile

Isopropyl Alcohol 70%

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

Product #33133

100 per box

INGREDIENTS AND APPEARANCE

MEDI-FIRST ALCOHOL WIPES 
isopropyl alcohol, 70% swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-331
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: 47682-331-33	100 in 1 BOX	07/01/2020	04/01/2025
1		0.4 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 47682-331-50	50 in 1 BOX	07/01/2020	04/01/2025
2		0.4 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	07/01/2020	04/01/2025

Labeler - Unifirst First Aid Corporation (832947092)