DERMFREE MEDICATED LIP- camphor 2.0%medicated lip ointment

DERMFREE MEDICATED LIP by

Drug Labeling and Warnings

DERMFREE MEDICATED LIP by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Camphor 2%

Purpose

xternal Analgesic

Use

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

Warnings

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

Do not use

Do not use on deep puncture wounds,serious burns, or animal bites. Keep out of reach of children. lfswallowed, get medical help or contact a Poison Control Center right away.

When Using

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

Stop Use

Stop use and ask a doctor if thecondition worsens or symptoms last more than 7 days or clear up andoccur again within a few days

Ask Doctor

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

Keep Oot Of Reach Of Children

If a child accidentally swallows it, please call the emergency center immediately.

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, etc.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMFREE MEDICATED LIP 
camphor 2.0%medicated lip ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-012
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)
GLYCERYL 2-CAPRYLATE (UNII: O8TCW8DUW8)
PROPYL ACETATE (UNII: 4AWM8C91G6)
PARAFFIN (UNII: I9O0E3H2ZE)
WHITE WAX (UNII: 7G1J5DA97F)
OLEAMIDE (UNII: 7L25QK8BWO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-012-01	10 g in 1 BOTTLE; Type 0: Not a Combination Product	04/29/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/29/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-012)