CHARMPOO ANTIFUNGAL CREAM- antifungal cream cream

Charmpoo Antifungal Cream by

Drug Labeling and Warnings

Charmpoo Antifungal Cream 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

miconazole nitrate 2% w/w

Purpose

Anti-fungal

Use

The product with Repairand Anti-ltch functioneffectivelyrelieve skindiscomfort, such asitching, athlete's footeczema, jockitch, et

Warnings

For external use only.Avoid direct contactwith eyes.

lfirritationoccurs,discontinue use.

Keep out of reach ofchildren.

Store in acool, darkplace

Do not use

For external use only.Avoid direct contactwith

When Using

1. First test a smallpatch of skin to checkfor any potentialallergicreaction.

2. Apply topically 2-3times daily to theaffected area.

Stop Use

Stop use and ask a doctor if irritation or rash occurs. There may besigns of a serious condition. Stop use if there is no improvement
within 4 weeks.

Ask Doctor

Stop use and ask a doctor if irritation or rash occurs. There may besigns of a serious condition. Stop use if there is no improvementwithin 4 weeks.

Keep Oot Of Reach Of Children

Keep it away from children. Seal the bottle and place it in acool and dry place.

Directions

1. First test a smallpatch of skin to checkfor any potentialallergicreaction

2. Apply topically 2-3times daily to the affected area.

Other information

Keep it away from children. Seal the bottle and place it in acool and dry place.

Inactive ingredients

Aloe, Borneol, Chlorhexidine acetate,Cnidium, Dictamnus,Euphorbia, Glycerin, Lightliquid paraffn, Medical vaseline,Natural menthol, Purifed water, Sophora Flavescens, Stearicacid, Stemona,Triethanolamine, Vitamin E

Questions

Email at support@charmpoo-intl.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CHARMPOO ANTIFUNGAL CREAM 
antifungal cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-009
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
STEMONA JAPONICA ROOT (UNII: FXG254HF10)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
EUPHORBIA NERIIFOLIA LEAF (UNII: IRZ1UXK5K9)
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
MENTHOL (UNII: L7T10EIP3A)
VASICINONE (UNII: G6T5819NXM)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
TROLAMINE (UNII: 9O3K93S3TK)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
STEARIC ACID (UNII: 4ELV7Z65AP)
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
GLYCERIN (UNII: PDC6A3C0OX)
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
BORNEOL (UNII: M89NIB437X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-009-01	100 g in 1 CANISTER; Type 0: Not a Combination Product	04/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	04/09/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	label(84010-009) , manufacture(84010-009)