NEKVNRO MEDICATED LIP OINTMENT.- medicated lip ointment ointment

Nekvnro Medicated Lip Ointment. by

Drug Labeling and Warnings

Nekvnro Medicated Lip Ointment. by is a Otc medication manufactured, distributed, or labeled by Guoyu Trading Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Camphor 2%

Purpose

External Analgesic

Use

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

Warnings

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

Do not use

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

When Using

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

Stop Use

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

Ask Doctor

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

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

Directions

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

Other information

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

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEKVNRO MEDICATED LIP OINTMENT. 
medicated lip ointment ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84844-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
PROPYL ACETATE (UNII: 4AWM8C91G6)
PARAFFIN (UNII: I9O0E3H2ZE)
WHITE WAX (UNII: 7G1J5DA97F)
GLYCERYL 2-CAPRYLATE (UNII: O8TCW8DUW8)
OLEAMIDE (UNII: 7L25QK8BWO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84844-004-01	10 g in 1 TUBE; Type 0: Not a Combination Product	10/31/2024
2	NDC: 84844-004-02	20 g in 1 TUBE; Type 0: Not a Combination Product	10/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/31/2024

Labeler - Guoyu Trading Co., Ltd. (963348600)

Establishment
Name	Address	ID/FEI	Business Operations
Guoyu Trading Co., Ltd.		963348600	manufacture(84844-004)