EVERCARE ANTIFUNGAL TREATMENT SUPER ABSORBENT POWDER- miconazole nitrate powder

Evercare Antifungal Treatment Super Absorbent Powder by

Drug Labeling and Warnings

Evercare Antifungal Treatment Super Absorbent Powder by is a Otc medication manufactured, distributed, or labeled by PANEFFORT, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Miconazole Nitrate 2%

Purpose

Antifungal

Use

for the cure of most athlete's foot (tinea pedis), jock itch (tinea cruris) and ringworm (tea corporis) for effective relief of itching, cracking, burning, scaling and discomfort

Warnings

For external use only.

Do not use while smoking or near heat or flame.  Flammable,

Do not use

on children under 2 years of age unless directed by a doctor

When using this product

• avoid contact with eyes. If product gets into eyes, rinse thoroughly with water.

Stop use and ask a doctor

if irritation occurs or there is no improvement within 4 weeks for athlete's foot and ringworm, or 2 weeks for jock itch

Keep out of reach of children.

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

Directions

clean the affected area& dry thoroughly apply a thin layerof the product over affected area twice daily (morning and night) or as directed by a doctor supervise children in the use of this product for athlete's foot: pay special attenting to spaces between the toes;wear wellfitting, ventilated shoes, & change shoes& socks at least once daily for athlete's foot&ringworm, use daily for 4 weeks, for jock itch, use daily for 2 weeks if condition persists longer, consult a doctor this product is not effective on the scalp or nails

Other information

store between 59-86 °F 

• lightly shake bottle to loosen settled powder

Inactive ingredients

corn starch, sodium bicarbonate, kaolin, zinc oxide, calamine

Package Labeling:

INGREDIENTS AND APPEARANCE

EVERCARE ANTIFUNGAL TREATMENT SUPER ABSORBENT POWDER 
miconazole nitrate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83099-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
KAOLIN (UNII: 24H4NWX5CO)
ZINC OXIDE (UNII: SOI2LOH54Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83099-000-00	85 g in 1 POUCH; Type 0: Not a Combination Product	11/28/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/28/2022

Labeler - PANEFFORT, LLC (018250858)