Nekvnro Anti-Itch Creme

Manufacturer
Guoyu Trading Co., Ltd.
Effective date
2024-10-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:33:36

Label at a glance#

ProductNekvnro Anti-Itch Creme
Active ingredientBEZLOTOXUMAB
Label structure12 sections

Dosage and administration

adults and children 12 years and older apply a fingertipamount (approximately 1-inch strip) to affected area not more than 3 to 4times daily.Clean nozzle of tube by wiping thoroughly before replacing cap.Keep cap tightly closed between uses. children under 12 years consult a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Bezocaine 5%

Purpose

OTC - PURPOSE SECTION

External analgesic

Use

INDICATIONS & USAGE SECTION

temporarily relieves itching

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Stop use and ask doctor if condition worsens, or if symptoms persist formore than 7 days, or clear up and occur again with in a few daysDo not apply over large areas of the body
Do not use if you have a vaginal discharge. Consult a physician.

When Using

OTC - WHEN USING SECTION

THIS PRODUCT Avoid contact with eyes

Stop Use

OTC - STOP USE SECTION

Stop use and ask doctor if condition worsens, or if symptoms persist formore than 7 days, or clear up and occur again with in a few daysDo not apply over large areas of the body
Do not use if you have a vaginal discharge. Consult a physician.

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and ask doctor if condition worsens, or if symptoms persist formore than 7 days, or clear up and occur again with in a few daysDo not apply over large areas of the body
Do not use if you have a vaginal discharge. Consult a physician.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years and older apply a fingertipamount (approximately 1-inch strip) to affected area not more than 3 to 4times daily.Clean nozzle of tube by wiping thoroughly before replacing cap.Keep cap tightly closed between uses.
children under 12 years consult a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerol 、Propylene Glycol 、Polydimethylsiloxane 、Trolaminewater、Boreol 、MENTHA PIPERITA、Methylparaben 、Chlorhexidine

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334455

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
3721525f-580a-45de-b4d6-2b95879548f9Product name120161213
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84844-007-01Nekvnro Anti-Itch Creme30 g in 1 TUBECREAM301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84844-007NEKVNRO ANTI-ITCH CREME (ANTI-ITCH CREME) CREAM [GUOYU TRADING CO., LTD.]11 package rows20241105_25c0b989-fad2-df81-e063-6394a90a4f02.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84844-00784844-007-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
25c0b989-fad3-df81-e063-6394a90a4f0225c0b989-fad2-df81-e063-6394a90a4f022024-10-31WarningsExact identifier
spl id: 25c0b989-fad3-df81-e063-6394a90a4f02
spl set id: 25c0b989-fad2-df81-e063-6394a90a4f02

Reported adverse events (FAERS/openFDA)#

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