Medicated Lip Ointment

Manufacturer
Guoyu Trading Co., Ltd.
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:33:35

Label at a glance#

ProductNekvnro Medicated Lip Ointment.
Active ingredientCAMPHOR (SYNTHETIC)
Label structure13 sections

Dosage and administration

· Apply to lips not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.

Storage and handling

This is a personal care item and should be used by one individual only.Inactive

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Camphor 2%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Use

INDICATIONS & USAGE SECTION

·Helps provide relief of symptoms of cold sores and dry lips.

Warnings

WARNINGS SECTION

·For external use only. When using this product, keep out of eyes. Rinse with water to remove.

Do not use

OTC - DO NOT USE SECTION

on deep puncture wounds, serious burns, or animal bites.

When Using

OTC - WHEN USING SECTION

this product, keep out of eyes. Rinse with water to remove.

Stop Use

OTC - STOP USE SECTION

if the condition worsens or symptoms last more than 7 days or clear up and occur again within a few days

Ask Doctor

OTC - ASK DOCTOR SECTION

if the condition worsens or symptoms last more than 7 days or clear up and occur again within a few days

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

· Apply to lips not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.

Other information

STORAGE AND HANDLING SECTION

This is a personal care item and should be used by one individual only.Inactive

Inactive ingredients

INACTIVE INGREDIENT SECTION

·Beeswax white, GLYCERYL 2-CAPRYLATE,Lanolin, Oleamide, Paraffin,Propyl Acetate

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334455667788991010

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2675876camphor 2 % Topical OintmentPSN1
2675876camphor 0.02 MG/MG Topical OintmentSCD1
2675876camphor 2 % Topical OintmentSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84844-004-012026-01-29C16284748780-149896155-b621-586f-e063-e6dba90add9084844-004
84844-004-022026-01-29C16284748780-149896155-b621-586f-e063-e6dba90add9084844-004

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84844-004-01Nekvnro Medicated Lip Ointment.10 g in 1 TUBEOINTMENT101
84844-004-02Nekvnro Medicated Lip Ointment.20 g in 1 TUBEOINTMENT201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84844-004NEKVNRO MEDICATED LIP OINTMENT. (MEDICATED LIP OINTMENT) OINTMENT [GUOYU TRADING CO., LTD.]12 package rows20241105_25bd4acc-a5fb-8f72-e063-6394a90ad876.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84844-00484844-004-01, 84844-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
25bd4acc-a5fc-8f72-e063-6394a90ad87625bd4acc-a5fb-8f72-e063-6394a90ad8762024-10-30WarningsExact identifier
spl id: 25bd4acc-a5fc-8f72-e063-6394a90ad876
spl set id: 25bd4acc-a5fb-8f72-e063-6394a90ad876

Reported adverse events (FAERS/openFDA)#

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