ZEASORB JOCK ITCH- miconazole nitrate powder 
Crown Laboratories

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Zeasorb Jock Itch

Active ingredient

Miconazole nitrate 2%

Purpose

Antifungal

Use

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

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

Zeasorb JI

ZEASORB JOCK ITCH 
miconazole nitrate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-8001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0316-8001-0271 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/19/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00510/19/2023
Labeler - Crown Laboratories (079035945)

Revised: 11/2023
Document Id: 09d088ef-aab3-5565-e063-6394a90af263
Set id: 09d088ef-aab3-5565-e063-6394a90af263
Version: 1
Effective Time: 20231110
 
Crown Laboratories