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NDC 47682-0212-12 Medi-First Antiseptic Wipes 1.33 mg/mL Details

Medi-First Antiseptic Wipes 1.33 mg/mL

Medi-First Antiseptic 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 BENZALKONIUM CHLORIDE.

Product Information

NDC	47682-0212
Product ID	47682-212_ebcbe75b-5283-2fa6-e053-2a95a90a3c0f
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 Antiseptic Wipes
Proprietary Name Suffix	n/a
Non-Proprietary Name	Benzalkonium chloride
Product Type	HUMAN OTC DRUG
Dosage Form	SWAB
Route	TOPICAL
Active Ingredient Strength	1.33
Active Ingredient Units	mg/mL
Substance Name	BENZALKONIUM CHLORIDE
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 47682-0212-12 (47682021212)

Pricing Information	N/A
NDC Package Code	47682-212-12
Billing NDC	47682021212
Package	10 PACKET in 1 BOX (47682-212-12) / 1.4 mL in 1 PACKET
Marketing Start Date	2017-08-21
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 5743634b-f329-5fec-e053-2991aa0a751d Details

Drug Facts

Active ingredient

Benzalkonium chloride 0.133% w/v

Purpose

First aid antiseptic

Uses

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

Warnings

Do not use

in the eyes or over large areas of the body
in case of deep or puncture woulds, animal bite or serious burns, consult a doctor
longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

if the condition persists or gets worse

Keep out of reach of children.

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

Directions

tear open packet, unfold and clean the affected area
discard after use
may be covered with a sterile bandage
if bandaged, let dry first

Other information

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

Inactive ingredients

sodium bicarbonate, water

Questions or comments?

1-800-634-7680

Medi-First Antiseptic Wipes Label

Medi-First®

Antiseptic Wipes

Benzalkonium chloride 0.133%

First aid Antiseptic

Product # 21412

Extra Large Wipes

Net Contents: 10 units per box

Medi-First Plus Antiseptic Wipes Label

Medi First ®

Plus

Antiseptic Wipes

Extra Large

Benzalkonium chloride 0.133% w/v

First Aid Antiseptic

Reorder # 103071

20 Wipes

INGREDIENTS AND APPEARANCE

MEDI-FIRST ANTISEPTIC WIPES

benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-212
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.33 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-212-12	10 in 1 BOX	08/21/2017
1		1.4 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-212-71	20 in 1 BOX	08/21/2017
2		1.4 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-212-33	100 in 1 BOX	08/21/2017
3		1.4 mL 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	08/21/2017

MEDI-FIRST PLUS ANTISEPTIC WIPES

benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-030
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-030-71	20 in 1 BOX	08/21/2017
1		1.4 mL 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	08/21/2017

Labeler - Unifirst First Aid Corporation (832947092)

Revised: 10/2022

Document Id: ebcbe75b-5283-2fa6-e053-2a95a90a3c0f

Set id: 5743634b-f329-5fec-e053-2991aa0a751d

Version: 7

Effective Time: 20221024