ZEASORB JOCK ITCH- miconazole nitrate powder

Zeasorb Jock Itch by

Drug Labeling and Warnings

Zeasorb Jock Itch by is a Otc medication manufactured, distributed, or labeled by Crown Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Use

• Proven clinically effective in the treament of most jock itch

Warnings

For external use only.

Avoid contact with the eyes.

Do not use

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

If irritation occurs or if there is no improvement within 2 weeks, discontinue use and consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a poison control center right away.

Directions

Wash the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. 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 at 20 o - 25 oC (68 o - 77 oF) [see USP Controlled Room Temperature]. Product settles during shipment. Package contains full net weight.

Inactive ingredients

Aloe Barbadensis Leaf Juice Powder, Bentonite, Fragrance, Potassium Sorbate, Sodium Benzoate, Tapioca Starch, Tricalcium Phosphate, Water, Zea Mays (Corn) Starch

Questions?

call 1-833-279-6522

Principal Display

New & Improved

Zeasorb®AF

Antifungal Powder

with 2% Miconazole Nitrate

Cures Most Jock Itch

Relieves Itching, Burning, Scaling

Patented Odor Control Technology

Attacks and Absorbs Moisture

Talc-Free, Paraben-Free, Aluminum-Free

Dermatologist Recommended

Net wt. 2.5 oz (71g)

P12322.00

INGREDIENTS AND APPEARANCE

ZEASORB JOCK ITCH 
miconazole nitrate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0316-8001
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
STARCH, TAPIOCA (UNII: 24SC3U704I)
TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
WATER (UNII: 059QF0KO0R)
STARCH, CORN (UNII: O8232NY3SJ)
BENTONITE (UNII: A3N5ZCN45C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0316-8001-02	71 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/19/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	10/19/2023

Labeler - Crown Laboratories (079035945)