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NDC 47682-0222-50 Medi-First Alcohol Wipes 0.7 mL/1 Details

Medi-First Alcohol Wipes 0.7 mL/1

Medi-First Alcohol Wipes is a TOPICAL SWAB in the HUMAN OTC DRUG category. It is labeled and distributed by Unifirst First Aid Corporation. The primary component is ISOPROPYL ALCOHOL.

Product Information

NDC	47682-0222
Product ID	47682-222_ebcb7fa5-faf4-8826-e053-2995a90a4d61
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Medi-First Alcohol Wipes
Proprietary Name Suffix	n/a
Non-Proprietary Name	Isopropyl Alcohol
Product Type	HUMAN OTC DRUG
Dosage Form	SWAB
Route	TOPICAL
Active Ingredient Strength	0.7
Active Ingredient Units	mL/1
Substance Name	ISOPROPYL ALCOHOL
Labeler Name	Unifirst First Aid Corporation
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part333A
Listing Certified Through	2023-12-31

Package

Package Images

NDC 47682-0222-50 (47682022250)

Pricing Information	N/A
NDC Package Code	47682-222-50
Billing NDC	47682022250
Package	50 PACKET in 1 BOX (47682-222-50) / 1 SWAB in 1 PACKET
Marketing Start Date	2017-05-09
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 3f507990-282a-4b26-e054-00144ff8d46c Details

Drug Facts

Active ingredient

Isopropyl alcohol, 70% v/v

Purpose

Antiseptic

Uses

for preparartion 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 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

store at room temperature 59°-86°F (15°-30°C)
tamper evidentsealed packets
do not use any open or torn packets

Inactive ingredient

purified water

Questions or comments?

Call 1-800-634-7680

Medi-First Alcohol Wipes Label

Medi-First®

Alcohol Wipes Sterile

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

Medium Sterile Wipes

100 per box

Medi-First Plus Alcohol Wipes Label

Medi-First Plus®

Alcohol Wipes

Sterile

Medium Sterile Wipes

50 per box

INGREDIENTS AND APPEARANCE

MEDI-FIRST ALCOHOL WIPES

isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-222
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-222-12	10 in 1 BOX	11/07/2016
1	NDC:47682-222-99	1 in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-222-50	50 in 1 BOX	05/09/2017
2		1 in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-222-33	100 in 1 BOX	05/09/2017
3		1 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	11/07/2016

MEDI-FIRST PLUS ALCOHOL WIPES

70% isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-031
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-031-50	50 in 1 BOX	06/23/2017
1		1 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	06/23/2017

Labeler - Unifirst First Aid Corporation (832947092)

Revised: 10/2022

Document Id: ebcb7fa5-faf4-8826-e053-2995a90a4d61

Set id: 3f507990-282a-4b26-e054-00144ff8d46c

Version: 8

Effective Time: 20221024