FDA.reportPublic FDA data

Zeasorb Jock Itch

Manufacturer
Crown Laboratories
Effective date
2026-01-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:32:23

Label at a glance#

ProductZeasorb Jock Itch
Active ingredientMICONAZOLE NITRATE
Label structure9 sections

Dosage and administration

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.

Storage and handling

store at 20 o - 25 o C (68 o - 77 o F) [see USP Controlled Room Temperature]. Product settles during shipment. Package contains full net weight.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconazole nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

  • Proven clinically effective in the treament of most jock itch

Warnings

WARNINGS SECTION

For external use only.

Avoid contact with the eyes.

Do not use

OTC - DO NOT USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

  • 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

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

call 1-833-279-6522

Principal Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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)

P12322.01

Zeasorb JIZeasorb JI

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998461miconazole nitrate 2 % Topical PowderPSN3
1437793Zeasorb 2 % Topical PowderPSN3
1437793miconazole nitrate 0.02 MG/MG Topical Powder [Zeasorb]SBD3
998461miconazole nitrate 0.02 MG/MG Topical PowderSCD3
998461miconazole nitrate 2 % Topical PowderSY3
1437793Zeasorb 0.02 MG/MG Topical PowderSY3
1437793Zeasorb 2 % Topical PowderSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MICONAZOLE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
3a55f4fb-5aec-4c88-0ff7-4d608ad4866aProduct name120140508
5b9a7965-36d2-8412-dcaf-f76a65411611Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0316-8001-02Zeasorb Jock Itch71 g in 1 BOTTLE, PLASTICPOWDER713

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0316-80010316-8001-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
MICONAZOLE NITRATEVW4H1CYW1KACTIB
SODIUM BENZOATEOJ245FE5EUIACT
STARCH, TAPIOCA24SC3U704IIACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
WATER059QF0KO0RIACT
STARCH, CORNO8232NY3SJIACT
BENTONITEA3N5ZCN45CIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-11-12monthly-update2026-06-03 17:39:04
12023-11-10full-release2026-05-31 23:59:47

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Zeasorb Jock ItchMICONAZOLE NITRATECrown Laboratories09d088ef-aab3-5565-e063-6394a90af2632026-01-12WarningsExact identifier
ndc (package): 0316-8001-02
ndc (product): 0316-8001
ndc11 (package): 00316800102
spl id: 4833f63f-c8ac-19bf-e063-6394a90abcdc
spl set id: 09d088ef-aab3-5565-e063-6394a90af263

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.