NEDTOL FOLLICULITIS TREATMENT CREAMS- miconazole nitrate cream

Nedtol Folliculitis Treatment Creams by

Drug Labeling and Warnings

Nedtol Folliculitis Treatment Creams by is a Otc medication manufactured, distributed, or labeled by Jiashen International Trade Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Miconazole Nitrate 2%.Anti-fungal

WARNINGS

FOR EXTERNAL USE ONLY.

DO NOT USE it on children under 2 yearsof age unless directed by a doctor.WHEN USING THIS PRODUCT,avoidcontact with the eyes, lf contact occurs,rinse the eyes very thoroughly with water.KEEP OUT OF THE REACH OF YOUING CHILDRENSTOP USING AND ASK A PHYSICIANif irritation occurs or there is noirmmprovement within 4 weeks,STOP USE AND ASK A DOCTORif discomfort persists.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF THE REACH OF YOUING CHILDREN

STOP USE

STOP USING AND ASK A PHYSICIANif irritation oocurs or there is no improwement within 4 weeks

PURPOSE

FOLLICULITISTINEA CAPITISLICHENPSORIASIS

INDICATIONS & USAGE

Treats most folliculitis,tinea capitis, Lichen,.and Psoriasis.Relieves the itching,irritation,redness,scaling,and discomfort accompanyingthese conditions.

DOSAGE & ADMINISTRATION

Wash the affectedarea and dry thorough-ly.Apply a thin layer over the affected areatwice daily ( morning and night ), or asdirected by a doctor,Supervise children inthe use of the product.lf the conditionpersists longer, consult a doctor.

OTHER SAFETY INFORMATION

OTHER INFORMATION
Store at 59-86F(15-30°C)Close the cap tightly after use.

INACTIVE INGREDIENT

Water
Camphor(SYNTHETIC)‌
Gentiana‌
Sophora Flavescens
Rhinacanthus Nasutus‌ ‌
Stemona Tuberosa Lour‌ ‌
Herba Violae‌ ‌
Euphorbia Hirta‌ ‌
Murraya Exotica‌ ‌
Peppermint‌ ‌
Glycerin‌
Methylparaben‌
Propylene Glycol‌
Silicone Oil‌
Triethanolamine‌

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NEDTOL FOLLICULITIS TREATMENT CREAMS 
miconazole nitrate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84867-022
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
RHINACANTHUS NASUTUS WHOLE (UNII: QW70YFP724)
VIOLA PATRINII (UNII: C1O8TSX4LG)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
GENTIANELLA AMARELLA ROOT (UNII: BZP57J2185)
MURRAYA PANICULATA LEAFY TWIG (UNII: VO9X9681W9)
TROLAMINE (UNII: 9O3K93S3TK)
DIMETHICONE (UNII: 92RU3N3Y1O)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
STEMONA TUBEROSA WHOLE (UNII: 9373ZOT316)
GLYCERIN (UNII: PDC6A3C0OX)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
EUPHORBIA HIRTA (UNII: L13YF113GN)
PEPPERMINT (UNII: V95R5KMY2B)
METHYLPARABEN (UNII: A2I8C7HI9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84867-022-01	120 g in 1 BOTTLE; Type 0: Not a Combination Product	08/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	08/23/2025

Labeler - Jiashen International Trade Limited (989067943)

Registrant - Jiashen International Trade Limited (989067943)