Bite and Sting Relief Wipe

Manufacturer: CVS | Diamond Wipes International, Inc.
Effective date: 2019-07-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:00:26

Label at a glance#

ProductBite and Sting Relief Wipe

Active ingredientALCOHOL, LIDOCAINE

Label structure8 sections

Indications and uses

First aid to help guard against skin infection and temporary relief of pain and itching assocaiated with insect bites.

Dosage and administration

Adults and children 2 years and older: Apply to clean affected area no more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 50.0%

Lidocaine HCL 2.0%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic
Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

First aid to help guard against skin infection and temporary relief of pain and itching assocaiated with insect bites.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

in the eyes over large areas of the body or bandage.
in large quantities particularly over raw surfaces or blistered areas.

Stop use and contact a doctor if the condition persists or worsens for more than 7 days or clears up and occurs again within a few days.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children if swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years and older: Apply to clean affected area no more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium Chloride, Menthol, Water.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Inner LabelOuter Box

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
LIDOCAINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
070fbed5-7088-434a-a7ce-f2a64d8d40ac	Product name	2	20260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80f	Product name	5	20250819
860a93dc-4863-49cc-b284-6bbe8191bc48	Product name	4	20250214
eaba870a-6a9d-442e-8643-87b3f558a451	Product name	1	20250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86	Product name	1	20230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57	Product name	3	20210602
aed701d5-9c75-dfaf-7154-cde46179faea	Product name	9	20200313
fa8b5901-e681-426f-82fe-54f6d81ec698	Product name	4	20180619
332d03e4-aa24-4b11-841a-02bf41081920	Product name	1	20171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070	Product name	1	20171221
68ed98f8-24c2-44a0-944a-6d36e82ce25a	Product name	1	20141222
1cd42bc2-a430-c72b-636d-991b235fbf80	Product name	1	20140508
49fa150c-f0de-cce7-3d9c-993ed81c5698	Product name	1	20140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ff	Product name	1	20140508
9137811f-f279-8640-5aeb-99fa2145d64d	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69842-190-10	2021-01-29	C162847	48780-1	ba0f9c33-1ec8-a910-e053-dadaa90a0b85	5360a3a5-a3ad-415b-bd9a-499c2472f95a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69842-190-10	Bite and Sting Relief Wipe	3 mL in 1 PACKET	Cloth	3		1
69842-190-10	Bite and Sting Relief Wipe	30 in 1 BOX	Cloth	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69842-190	BITE AND STING RELIEF WIPE (ALCOHOL 50% LIDOCAINE HCL 2%) CLOTH [CVS]	1	Legacy NDC, 2 package rows	20190917_5360a3a5-a3ad-415b-bd9a-499c2472f95a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Bite and Sting Relief Wipe
Alcohol 50% Lidocaine HCL 2%
ALCOHOL
LIDOCAINE
BENZALKONIUM CHLORIDE
MENTHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69842-190	69842-190-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
LIDOCAINE	98PI200987	ACTIB
BENZALKONIUM CHLORIDE	F5UM2KM3W7	IACT
MENTHOL	L7T10EIP3A	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
3bd85882-7bb7-4490-8390-3bee8f0256c9			5360a3a5-a3ad-415b-bd9a-499c2472f95a	2019-07-05	Warnings	Exact identifier spl id: 3bd85882-7bb7-4490-8390-3bee8f0256c9 spl set id: 5360a3a5-a3ad-415b-bd9a-499c2472f95a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.