NERANTE ANTIFUNGAL CREAM- miconazole nitrate, hydrocortisone cream

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Miconazole Nitrate 2%
Hydrocortisone 0.3%

PURPOSE

Antifungal
Anti-Itch

INDICATIONS & USAGE

Cures most athlete's foot between the toes.

Effectiveness on the bottom or sides of foot is unknown.

Cures most jock itch and ringworm.

Relieves itching, burning, cracking, and scaling which accompany these conditions.

WARNINGS

For external use only.
Ask a doctor before use if pregnant or nursing.

DO NOT USE

Do not use on nails or scalp.
Do not use if allergic to any ingredients in this product.
Do not use in or near the mouth or the eyes.
Do not use for vaginal yeast infections.

WHEN USING

When using this product, avoid contact with eyes, noseand mouth. If contact occurs, rinse thoroughly with water.

STOP USE

Stop using and ask a doctor if too much irritation occurs or irritation gets worse.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidentalingestion, get medical help or contact a poison control centerimmediately.

DOSAGE & ADMINISTRATION

For adults and children 12 years and older:
1.Wash and dry the affected area before application.
2.Athlete's Foot (between toes): Apply a thin layer to the affected area between and around the toes. Use twice daily (morning and night) for 1 week, or once daily for 2 weeks,or as directed by a doctor. Wear well-fitting, ventilatedshoes and change shoes and socks at least once daily.
3.Jock Itch and Ringworm: Apply a thin layer to the affected area once daily for 1 week, or as directed by a doctor.
4.Wash hands after use.
Children under 12 years: Ask a doctor.

INACTIVE INGREDIENT

WATER
CETYL ALCOHOL
STEARYL ALCOHOL
GLYCERYL STEARATE
GLYCERIN
MINERAL OIL
CETEARETH-25
STEARIC ACID
ETHYLHEXYL PALMITATE
CAMPHOR
MENTHOL
GENTIANA SCABRA EXTRACT
BUTYLENE GLYCOL
HYDROXYACETOPHENONE
CENTELLA ASIATICA EXTRACT
AVENA SATIVA (OAT) KERNEL EXTRACT
ROSA RUGOSA FLOWER EXTRACT
LACTOBACILLUS FERMENT
BUTYLENE GLYCOL
DIMETHICONE
GLYCERYL CAPRYLATE
HYDROXYACETOPHENONE
ETHYLHEXYLGLYCERIN
1,2-HEXANEDIOL
ALLANTOIN
POTASSIUM LAURYL PHOSPHATE
DIPOTASSIUM PHOSPHATE
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
XANTHAN GUM
BUTYLENE GLYCOL
PENTYLENE GLYCOL
HYDROXYPHENYL PROPAMIDOBENZOIC ACID
ASCORBYL PALMITATE
TRIETHANOLAMINE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NERANTE ANTIFUNGAL CREAM 
miconazole nitrate, hydrocortisone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87681-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	0.003 g  in 1 g
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	0.02 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
ALLANTOIN (UNII: 344S277G0Z)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CETEARETH-25 (UNII: 8FA93U5T67)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIMETHICONE (UNII: 92RU3N3Y1O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POTASSIUM LAURYL PHOSPHATE (UNII: C4QT53N4MK)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
XANTHAN GUM (UNII: TTV12P4NEE)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
OAT (UNII: Z6J799EAJK)
ROSA RUGOSA FLOWER (UNII: 969IQC5YJU)
DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
MENTHOL (UNII: L7T10EIP3A)
GLYCERIN (UNII: PDC6A3C0OX)
MINERAL OIL (UNII: T5L8T28FGP)
GENTIANA SCABRA WHOLE (UNII: 06T1X86LXT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87681-001-01	2 in 1 BOX	05/19/2026
1		15 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	05/19/2026

Labeler - Guangzhou Xinhongda Trading Service Co., Ltd. (704975103)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Xinhongda Trading Service Co., Ltd.		704975103	manufacture(87681-001)