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NDC 47682-0234-12 Medi-First Sting Relief 60; .6 mg/mL; mL/mL Details

Medi-First Sting Relief 60; .6 mg/mL; mL/mL

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

Product Information

NDC	47682-0234
Product ID	47682-234_ebccfeba-addc-c1d9-e053-2995a90aa746
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 Sting Relief
Proprietary Name Suffix	n/a
Non-Proprietary Name	Benzocaine 6%, Isopropyl alcohol 60%
Product Type	HUMAN OTC DRUG
Dosage Form	SWAB
Route	TOPICAL
Active Ingredient Strength	60; .6
Active Ingredient Units	mg/mL; mL/mL
Substance Name	BENZOCAINE; ISOPROPYL ALCOHOL
Labeler Name	Unifirst First Aid Corporation
Pharmaceutical Class	Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part348
Listing Certified Through	2023-12-31

Package

Package Images

NDC 47682-0234-12 (47682023412)

Pricing Information	N/A
NDC Package Code	47682-234-12
Billing NDC	47682023412
Package	10 PACKET in 1 BOX (47682-234-12) / .6 mL in 1 PACKET
Marketing Start Date	2018-07-02
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 6e610821-b030-930b-e053-2a91aa0a66f9 Details

Drug Facts

Active ingredient

Benzocaine 6% w/v

Isopropyl alcohol 60% w/v

Purpose

Topical anesthetic

Antiseptic

Uses

For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

in the eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

irritation, redness or other symptoms develop
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

Adults and children 2 years of age and older: Apply to affected area 3-4 times daily.

Children under 2 years: CXonsult physician.

Other information

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

Inactive ingredients

purified water

Questions or comments?

1-800-634-7680

Medi-First Sting Relief Wipes Label

Medi-First®

Sting Relief Wipes

Benzocaine/ Isopropyl Acohol

Topical Anesthetic/ Antiseptic

Product # 23112

NET CONTENTS: 10 wipes per box

INGREDIENTS AND APPEARANCE

MEDI-FIRST STING RELIEF

benzocaine 6%, isopropyl alcohol 60% swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-234
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	60 mg in 1 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.6 mL in 1 mL

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-234-99	0.6 mL in 1 PACKET; Type 0: Not a Combination Product	07/02/2018
2	NDC:47682-234-12	10 in 1 BOX	07/02/2018
2		0.6 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	part348	07/02/2018

Labeler - Unifirst First Aid Corporation (832947092)

Revised: 10/2022

Document Id: ebccfeba-addc-c1d9-e053-2995a90aa746

Set id: 6e610821-b030-930b-e053-2a91aa0a66f9

Version: 5

Effective Time: 20221024